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Volumn 115, Issue 11, 2015, Pages 5366-5412

Erratum: Recent Advances of Catalytic Asymmetric 1,3-Dipolar Cycloadditions (Chemical Reviews (2015) 115:11 (5366-5412) DOI:10.1021/cr5007182));Recent Advances of Catalytic Asymmetric 1,3-Dipolar Cycloadditions

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EID: 84935873660     PISSN: 00092665     EISSN: 15206890     Source Type: Journal    
DOI: 10.1021/acs.chemrev.5b00387     Document Type: Erratum
Times cited : (851)

References (433)
  • 1
    • 36749014055 scopus 로고
    • 1,3-Dipolar Cycloadditions. Past and Future
    • Huisgen, R. 1,3-Dipolar Cycloadditions. Past and Future Angew. Chem., Int. Ed. Engl. 1963, 2, 565 - 598
    • (1963) Angew. Chem., Int. Ed. Engl. , vol.2 , pp. 565-598
    • Huisgen, R.1
  • 2
    • 0000299952 scopus 로고
    • Kinetics and Mechanism of 1,3-Dipolar Cycloadditions
    • Huisgen, R. Kinetics and Mechanism of 1,3-Dipolar Cycloadditions Angew. Chem., Int. Ed. Engl. 1963, 2, 633 - 645
    • (1963) Angew. Chem., Int. Ed. Engl. , vol.2 , pp. 633-645
    • Huisgen, R.1
  • 3
    • 11544346529 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition Reactions
    • Gothelf, K. V.; Jorgensen, K. A. Asymmetric 1,3-Dipolar Cycloaddition Reactions Chem. Rev. 1998, 98, 863 - 910
    • (1998) Chem. Rev. , vol.98 , pp. 863-910
    • Gothelf, K.V.1    Jorgensen, K.A.2
  • 4
    • 0036373830 scopus 로고    scopus 로고
    • Metal-Assisted Stereocontrol of 1,3-Dipolar Cycloaddition Reactions
    • Kanemasa, S. Metal-Assisted Stereocontrol of 1,3-Dipolar Cycloaddition Reactions Synlett 2002, 1371 - 1387
    • (2002) Synlett , pp. 1371-1387
    • Kanemasa, S.1
  • 5
    • 79751521759 scopus 로고    scopus 로고
    • Cornerstone Works for Catalytic 1,3-Dipolar Cycloaddition Reactions
    • Kanemasa, S. Cornerstone Works for Catalytic 1,3-Dipolar Cycloaddition Reactions Heterocycles 2010, 82, 87 - 200
    • (2010) Heterocycles , vol.82 , pp. 87-200
    • Kanemasa, S.1
  • 6
    • 33947231700 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloadditions
    • Pellissier, H. Asymmetric 1,3-Dipolar Cycloadditions Tetrahedron 2007, 63, 3235 - 3285
    • (2007) Tetrahedron , vol.63 , pp. 3235-3285
    • Pellissier, H.1
  • 7
    • 51049094424 scopus 로고    scopus 로고
    • Enantioselective Copper-Catalyzed 1,3-Dipolar Cycloadditions
    • Stanley, L. M.; Sibi, M. P. Enantioselective Copper-Catalyzed 1,3-Dipolar Cycloadditions Chem. Rev. 2008, 108, 2887 - 2902
    • (2008) Chem. Rev. , vol.108 , pp. 2887-2902
    • Stanley, L.M.1    Sibi, M.P.2
  • 8
    • 44649151639 scopus 로고    scopus 로고
    • Asymmetric Lewis Acid-Catalyzed 1,3-Dipolar Cycloadditions
    • Bədoiu, A.; Brinkmann, Y.; Viton, F.; Kündig, E. P. Asymmetric Lewis Acid-Catalyzed 1,3-Dipolar Cycloadditions Pure Appl. Chem. 2008, 80, 1013 - 1018
    • (2008) Pure Appl. Chem. , vol.80 , pp. 1013-1018
    • Bədoiu, A.1    Brinkmann, Y.2    Viton, F.3    Kündig, E.P.4
  • 9
    • 57749088567 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition Reactions Using Chiral Lanthanide Catalysts
    • Golebiewski, W. M.; Gucma, M. Enantioselective 1,3-Dipolar Cycloaddition Reactions Using Chiral Lanthanide Catalysts J. Heterocycl. Chem. 2008, 45, 1687 - 1693
    • (2008) J. Heterocycl. Chem. , vol.45 , pp. 1687-1693
    • Golebiewski, W.M.1    Gucma, M.2
  • 10
    • 75749125834 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloadditions of Acrylamides
    • Kissane, M.; Maguire, A. R. Asymmetric 1,3-Dipolar Cycloadditions of Acrylamides Chem. Soc. Rev. 2010, 39, 845 - 883
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 845-883
    • Kissane, M.1    Maguire, A.R.2
  • 11
    • 77951788015 scopus 로고    scopus 로고
    • Metal Complexes Versus Organocatalysts in Asymmetric 1,3-Dipolar Cycloadditions
    • Nájera, C.; Sansano, J. M.; Yus, M. Metal Complexes Versus Organocatalysts in Asymmetric 1,3-Dipolar Cycloadditions J. Braz. Chem. Soc. 2010, 21, 377 - 412
    • (2010) J. Braz. Chem. Soc. , vol.21 , pp. 377-412
    • Nájera, C.1    Sansano, J.M.2    Yus, M.3
  • 12
    • 84859714447 scopus 로고    scopus 로고
    • Organocatalytic and Metal-Mediated Asymmetric [3 + 2] Cycloaddition Reactions
    • Xing, Y.; Wang, N.-X. Organocatalytic and Metal-Mediated Asymmetric [3 + 2] Cycloaddition Reactions Coord. Chem. Rev. 2012, 256, 938 - 952
    • (2012) Coord. Chem. Rev. , vol.256 , pp. 938-952
    • Xing, Y.1    Wang, N.-X.2
  • 13
    • 0034699058 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloaddition Reactions of Nitrones
    • Gothelf, K. V.; Jorgensen, K. A. Catalytic Enantioselective 1,3-Dipolar Cycloaddition Reactions of Nitrones Chem. Commun. 2000, 1449 - 1458
    • (2000) Chem. Commun. , pp. 1449-1458
    • Gothelf, K.V.1    Jorgensen, K.A.2
  • 14
    • 33751553196 scopus 로고
    • Tungstate-Catalyzed Oxidation of Secondary Amines to Nitrones. α-Substitution of Secondary Amines via Nitrones
    • Murahashi, S.-I.; Mitsui, H.; Shiota, T.; Tsuda, T.; Watanabe, S. Tungstate-Catalyzed Oxidation of Secondary Amines to Nitrones. α-Substitution of Secondary Amines via Nitrones J. Org. Chem. 1990, 55, 1736 - 1744
    • (1990) J. Org. Chem. , vol.55 , pp. 1736-1744
    • Murahashi, S.-I.1    Mitsui, H.2    Shiota, T.3    Tsuda, T.4    Watanabe, S.5
  • 15
    • 0000104422 scopus 로고
    • Transition-Metal Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Alkenes and Nitrones
    • Gothelf, K. V.; Jorgensen, K. A. Transition-Metal Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Alkenes and Nitrones J. Org. Chem. 1994, 59, 5687 - 5691 See also ref 3.
    • (1994) J. Org. Chem. , vol.59 , pp. 5687-5691
    • Gothelf, K.V.1    Jorgensen, K.A.2
  • 16
    • 0030581362 scopus 로고    scopus 로고
    • Palladium-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Olefins
    • Hori, K.; Kodama, H.; Ohta, T.; Furukawa, I. Palladium-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Olefins Tetrahedron Lett. 1996, 37, 5947 - 5950
    • (1996) Tetrahedron Lett. , vol.37 , pp. 5947-5950
    • Hori, K.1    Kodama, H.2    Ohta, T.3    Furukawa, I.4
  • 17
    • 0032997310 scopus 로고    scopus 로고
    • Palladium(II)-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to 3-Alkenoyl-1,3-oxazolidin-2-ones
    • Hori, K.; Kodama, H.; Ohta, T.; Furukawa, I. Palladium(II)-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to 3-Alkenoyl-1,3-oxazolidin-2-ones J. Org. Chem. 1999, 64, 5017 - 5023
    • (1999) J. Org. Chem. , vol.64 , pp. 5017-5023
    • Hori, K.1    Kodama, H.2    Ohta, T.3    Furukawa, I.4
  • 18
    • 0002065863 scopus 로고    scopus 로고
    • Lanthanide-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Alkenes Using 3,3′-Bis(2-oxazolyl)-1,1′-bi-2-naphthol (BINOL-Box) Ligands
    • Kodama, H.; Ito, J.; Hori, K.; Ohta, T.; Furukawa, I. Lanthanide-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Alkenes Using 3,3′-Bis(2-oxazolyl)-1,1′-bi-2-naphthol (BINOL-Box) Ligands J. Organomet. Chem. 2000, 603, 6 - 12
    • (2000) J. Organomet. Chem. , vol.603 , pp. 6-12
    • Kodama, H.1    Ito, J.2    Hori, K.3    Ohta, T.4    Furukawa, I.5
  • 19
    • 0032540703 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloadditions between Nitrones and Alkenes Using a Novel Heterochiral Ytterbium(III) Catalyst
    • Kobayashi, S.; Kawamura, M. Catalytic Enantioselective 1,3-Dipolar Cycloadditions between Nitrones and Alkenes Using a Novel Heterochiral Ytterbium(III) Catalyst J. Am. Chem. Soc. 1998, 120, 5840 - 5841
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5840-5841
    • Kobayashi, S.1    Kawamura, M.2
  • 20
    • 0032477318 scopus 로고    scopus 로고
    • Highly Endo- and Enantioselective Asymmetric Nitrone Cycloadditions Catalyzed by the Aqua Complex of 4,6-Dibenzofurandiyl-2,2‘-bis(4-phenyl-oxazoline)-Nickel(II) Perchlorate. Transition Structure Based on Dramatic Effect of MS 4A on Selectivities
    • Kanemasa, S.; Oderaotoshi, Y.; Tanaka, J.; Wada, E. Highly Endo- and Enantioselective Asymmetric Nitrone Cycloadditions Catalyzed by the Aqua Complex of 4,6-Dibenzofurandiyl-2,2‘-bis(4-phenyl-oxazoline)-Nickel(II) Perchlorate. Transition Structure Based on Dramatic Effect of MS 4A on Selectivities J. Am. Chem. Soc. 1998, 120, 12355 - 12356
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 12355-12356
    • Kanemasa, S.1    Oderaotoshi, Y.2    Tanaka, J.3    Wada, E.4
  • 21
    • 0033525650 scopus 로고    scopus 로고
    • 1,3-Dipolar Cycloadditions Catalyzed by Bis(oxazoline)-Magnesium-Based Chiral Complexes. The Importance of a Mg(II) Counterion
    • Desimoni, G.; Faita, G.; Mortoni, A.; Righetti, P. 1,3-Dipolar Cycloadditions Catalyzed by Bis(oxazoline)-Magnesium-Based Chiral Complexes. The Importance of a Mg(II) Counterion Tetrahedron Lett. 1999, 40, 2001 - 2004
    • (1999) Tetrahedron Lett. , vol.40 , pp. 2001-2004
    • Desimoni, G.1    Faita, G.2    Mortoni, A.3    Righetti, P.4
  • 22
    • 0033578838 scopus 로고    scopus 로고
    • Chiral Amplification in Diels-Alder and 1,3-Dipolar Cycloadditions Catalyzed by Bis(oxazoline)-Zn(II)-Based Chiral Complexes
    • Crosignani, S.; Desimoni, G.; Faita, G.; Filippone, S.; Mortoni, A.; Righetti, P.; Zema, M. Chiral Amplification in Diels-Alder and 1,3-Dipolar Cycloadditions Catalyzed by Bis(oxazoline)-Zn(II)-Based Chiral Complexes Tetrahedron Lett. 1999, 40, 7007 - 7010
    • (1999) Tetrahedron Lett. , vol.40 , pp. 7007-7010
    • Crosignani, S.1    Desimoni, G.2    Faita, G.3    Filippone, S.4    Mortoni, A.5    Righetti, P.6    Zema, M.7
  • 23
    • 15944368088 scopus 로고    scopus 로고
    • In Search of exo-Selective Catalysts for Enantioselective 1,3-Dipolar Cycloaddition between Acryloyloxazolidinone and Diphenylnitrone
    • Desimoni, G.; Faita, G.; Mella, M.; Boiocchi, M. In Search of exo-Selective Catalysts for Enantioselective 1,3-Dipolar Cycloaddition between Acryloyloxazolidinone and Diphenylnitrone Eur. J. Org. Chem. 2005, 1020 - 1027
    • (2005) Eur. J. Org. Chem. , pp. 1020-1027
    • Desimoni, G.1    Faita, G.2    Mella, M.3    Boiocchi, M.4
  • 24
    • 70450195050 scopus 로고    scopus 로고
    • II/Isopropylidene-2,2-Bis(oxazoline) Catalyst and Its Stable Reactive Complex with Acryloyloxazolidinone in Enantioselective Reactions
    • II/Isopropylidene-2,2-Bis(oxazoline) Catalyst and Its Stable Reactive Complex with Acryloyloxazolidinone in Enantioselective Reactions Chem.-Eur. J. 2009, 15, 9674 - 9677
    • (2009) Chem. - Eur. J. , vol.15 , pp. 9674-9677
    • Desimoni, G.1    Faita, G.2    Toscanini, M.3    Boiocchi, M.4
  • 25
    • 0035903952 scopus 로고    scopus 로고
    • Synthesis of 2,6-Bis(4R-trialkylsiloxymethyloxazolinyl)pyridines and their Use in Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reactions of Nitrones and Activated Alkenes
    • Iwasa, S.; Tsushima, S.; Shimada, T.; Nishiyama, H. Synthesis of 2,6-Bis(4R-trialkylsiloxymethyloxazolinyl)pyridines and their Use in Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reactions of Nitrones and Activated Alkenes Tetrahedron Lett. 2001, 42, 6715 - 6717
    • (2001) Tetrahedron Lett. , vol.42 , pp. 6715-6717
    • Iwasa, S.1    Tsushima, S.2    Shimada, T.3    Nishiyama, H.4
  • 26
    • 0037033563 scopus 로고    scopus 로고
    • Chiral Bis(trialkylsiloxymethyloxazolinyl)pyridine ligands. Highly Enantioselective 1,3-Dipolar Cycloaddition Reactions
    • Iwasa, S.; Tsushima, S.; Shimada, T.; Nishiyama, H. Chiral Bis(trialkylsiloxymethyloxazolinyl)pyridine ligands. Highly Enantioselective 1,3-Dipolar Cycloaddition Reactions Tetrahedron 2002, 58, 227 - 232
    • (2002) Tetrahedron , vol.58 , pp. 227-232
    • Iwasa, S.1    Tsushima, S.2    Shimada, T.3    Nishiyama, H.4
  • 27
    • 0037037937 scopus 로고    scopus 로고
    • A Highly Enantioselective 1,3-Dipolar Cycloaddition Reaction in Alcoholic Media: Ni(II)-Pybox-Tipsom Catalyst
    • Iwasa, S.; Maeda, H.; Nishiyama, K.; Tsushima, S.; Tsukamoto, Y.; Nishiyama, H. A Highly Enantioselective 1,3-Dipolar Cycloaddition Reaction in Alcoholic Media: Ni(II)-Pybox-Tipsom Catalyst Tetrahedron 2002, 58, 8281 - 8287
    • (2002) Tetrahedron , vol.58 , pp. 8281-8287
    • Iwasa, S.1    Maeda, H.2    Nishiyama, K.3    Tsushima, S.4    Tsukamoto, Y.5    Nishiyama, H.6
  • 28
    • 1242272933 scopus 로고    scopus 로고
    • Synthesis of Novel Chiral Bis(2-oxazolinyl)xanthene (Xabox) Ligands and their Evaluation in Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reactions of Nitrones with 3-Crotonoyl-2-oxazolidinone
    • Iwasa, S.; Ishima, Y.; Widagdo, H. S.; Aoki, K.; Nishiyama, H. Synthesis Of Novel Chiral Bis(2-oxazolinyl)xanthene (Xabox) Ligands and their Evaluation in Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reactions of Nitrones with 3-Crotonoyl-2-oxazolidinone Tetrahedron Lett. 2004, 45, 2121 - 2124
    • (2004) Tetrahedron Lett. , vol.45 , pp. 2121-2124
    • Iwasa, S.1    Ishima, Y.2    Widagdo, H.S.3    Aoki, K.4    Nishiyama, H.5
  • 29
    • 38349035569 scopus 로고    scopus 로고
    • Chiral Bis(2-oxazolinyl)xanthene (Xabox)/Transition-Metal Complexes Catalyzed 1,3-Dipolar Cycloaddition Reactions and Diels-Alder Reactions
    • Phomkeona, K.; Takemoto, T.; Ishima, Y.; Shibatomi, K.; Iwasa, S.; Nishiyama, H. Chiral Bis(2-oxazolinyl)xanthene (Xabox)/Transition-Metal Complexes Catalyzed 1,3-Dipolar Cycloaddition Reactions and Diels-Alder Reactions Tetrahedron 2008, 64, 1813 - 1822
    • (2008) Tetrahedron , vol.64 , pp. 1813-1822
    • Phomkeona, K.1    Takemoto, T.2    Ishima, Y.3    Shibatomi, K.4    Iwasa, S.5    Nishiyama, H.6
  • 30
    • 0037245780 scopus 로고    scopus 로고
    • Enantio- and Diastereoselectivity in 1,3-Dipolar Cycloaddition Reactions of Nitrones with 3-Crotonoyl-2-oxazolidinone Catalyzed by Ni(II)- Binaphthyldiimine Complexes
    • Suga, H.; Kakehi, A.; Ito, S.; Sugimoto, H. Enantio- and Diastereoselectivity in 1,3-Dipolar Cycloaddition Reactions of Nitrones with 3-Crotonoyl-2-oxazolidinone Catalyzed by Ni(II)- Binaphthyldiimine Complexes Bull. Chem. Soc. Jpn. 2003, 76, 327 - 334
    • (2003) Bull. Chem. Soc. Jpn. , vol.76 , pp. 327-334
    • Suga, H.1    Kakehi, A.2    Ito, S.3    Sugimoto, H.4
  • 31
    • 9644294409 scopus 로고    scopus 로고
    • Evaluation of Chiral Bidentate Ligand-Metal Complexes in Asymmetric 1,3-Dipolar Cycloaddition Reaction of Nitrones with 3-Alkenoyl-2-Oxazolidinones
    • Saito, T.; Yamada, T.; Miyazaki, S.; Otani, T. Evaluation of Chiral Bidentate Ligand-Metal Complexes in Asymmetric 1,3-Dipolar Cycloaddition Reaction of Nitrones with 3-Alkenoyl-2-Oxazolidinones Tetrahedron Lett. 2004, 45, 9581 - 9584
    • (2004) Tetrahedron Lett. , vol.45 , pp. 9581-9584
    • Saito, T.1    Yamada, T.2    Miyazaki, S.3    Otani, T.4
  • 32
    • 9644266910 scopus 로고    scopus 로고
    • Catalytic Highly Enantioselective 1,3-Dipolar Cycloaddition Reaction of Nitrones with 3-Alkenoyl-2-Oxazolidinones by Use of a Bidentate Chiral Bis(imine) Ligand-Cu(II) Triflate Complex
    • Saito, T.; Yamada, T.; Miyazaki, S.; Otani, T. Catalytic Highly Enantioselective 1,3-Dipolar Cycloaddition Reaction of Nitrones with 3-Alkenoyl-2-Oxazolidinones by Use of a Bidentate Chiral Bis(imine) Ligand-Cu(II) Triflate Complex Tetrahedron Lett. 2004, 45, 9585 - 9587
    • (2004) Tetrahedron Lett. , vol.45 , pp. 9585-9587
    • Saito, T.1    Yamada, T.2    Miyazaki, S.3    Otani, T.4
  • 33
    • 25844444557 scopus 로고    scopus 로고
    • Lewis Acid Catalyzed Asymmetric Cycloadditions of Nitrones: α′-Hydroxy Enones as Efficient Reaction Partners
    • Palomo, C.; Oiarbide, M.; Arceo, E.; García, J. M.; López, R.; González, A.; Linden, A. Lewis Acid Catalyzed Asymmetric Cycloadditions of Nitrones: α′-Hydroxy Enones as Efficient Reaction Partners Angew. Chem., Int. Ed. 2005, 44, 6187 - 6190
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 6187-6190
    • Palomo, C.1    Oiarbide, M.2    Arceo, E.3    García, J.M.4    López, R.5    González, A.6    Linden, A.7
  • 34
    • 33746879548 scopus 로고    scopus 로고
    • Enantioselective Nitrone Cycloadditions of α,β-Unsaturated 2-Acyl Imidazoles Catalyzed by Bis(oxazolinyl)pyridine-Cerium(IV) Triflate Complexes
    • Evans, D. A.; Song, H.-J.; Fandrick, K. R. Enantioselective Nitrone Cycloadditions of α,β-Unsaturated 2-Acyl Imidazoles Catalyzed by Bis(oxazolinyl)pyridine-Cerium(IV) Triflate Complexes Org. Lett. 2006, 8, 3351 - 3354
    • (2006) Org. Lett. , vol.8 , pp. 3351-3354
    • Evans, D.A.1    Song, H.-J.2    Fandrick, K.R.3
  • 35
    • 53949101584 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reaction of Nitrones with α′-Phosphoric Enones by a Chiral Ligand-Copper(II) Triflate Complex
    • Lim, K.-C.; Hong, Y.-T.; Kim, S. Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reaction of Nitrones with α′-Phosphoric Enones by a Chiral Ligand-Copper(II) Triflate Complex Adv. Synth. Catal. 2008, 350, 380 - 384
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 380-384
    • Lim, K.-C.1    Hong, Y.-T.2    Kim, S.3
  • 36
    • 79851471445 scopus 로고    scopus 로고
    • Highly Enantioselective Nitrone Cycloadditions with 2-Alkenoyl Pyridine N-Oxides Catalyzed by Cu
    • Barroso, S.; Blay, G.; Muñoz, M. C.; Pedro, J. R. Highly Enantioselective Nitrone Cycloadditions with 2-Alkenoyl Pyridine N-Oxides Catalyzed by Cu Org. Lett. 2011, 13, 402 - 405
    • (2011) Org. Lett. , vol.13 , pp. 402-405
    • Barroso, S.1    Blay, G.2    Muñoz, M.C.3    Pedro, J.R.4
  • 37
    • 1642535360 scopus 로고    scopus 로고
    • Exo Selective Enantioselective Nitrone Cycloadditions
    • Sibi, M. P.; Ma, Z.; Jasperse, C. P. Exo Selective Enantioselective Nitrone Cycloadditions J. Am. Chem. Soc. 2004, 126, 718 - 719
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 718-719
    • Sibi, M.P.1    Ma, Z.2    Jasperse, C.P.3
  • 38
    • 20544472149 scopus 로고    scopus 로고
    • Enantioselective Cycloadditions with α,β-Disubstituted Acrylimides
    • Sibi, M. P.; Ma, Z.; Itoh, K.; Prabagaran, N.; Jasperse, C. P. Enantioselective Cycloadditions with α,β-Disubstituted Acrylimides Org. Lett. 2005, 7, 2349 - 2352
    • (2005) Org. Lett. , vol.7 , pp. 2349-2352
    • Sibi, M.P.1    Ma, Z.2    Itoh, K.3    Prabagaran, N.4    Jasperse, C.P.5
  • 39
    • 17444374300 scopus 로고    scopus 로고
    • Highly Exo-Selective and Enantioselective Cycloaddition Reactions of Nitrones Catalyzed by a Chiral Binaphthyldiimine-Ni(II) Complex
    • Suga, H.; Nakajima, T.; Itoh, K.; Kakehi, A. Highly Exo-Selective and Enantioselective Cycloaddition Reactions of Nitrones Catalyzed by a Chiral Binaphthyldiimine-Ni(II) Complex Org. Lett. 2005, 7, 1431 - 1434
    • (2005) Org. Lett. , vol.7 , pp. 1431-1434
    • Suga, H.1    Nakajima, T.2    Itoh, K.3    Kakehi, A.4
  • 40
    • 2542592576 scopus 로고    scopus 로고
    • Diastereoselectivity-Switchable and Highly Enantioselective 1,3-Dipolar Cycloaddition of Nitrones to Alkylidene Malonates
    • Huang, Z.-Z.; Kang, Y.-B.; Zhou, J.; Ye, M.-C.; Tang, Y. Diastereoselectivity-Switchable and Highly Enantioselective 1,3-Dipolar Cycloaddition of Nitrones to Alkylidene Malonates Org. Lett. 2004, 6, 1677 - 1679
    • (2004) Org. Lett. , vol.6 , pp. 1677-1679
    • Huang, Z.-Z.1    Kang, Y.-B.2    Zhou, J.3    Ye, M.-C.4    Tang, Y.5
  • 41
    • 79955012730 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Alkylidene Malonates: Highly Enantioselective Synthesis of Multisubstituted Isoxazolidines
    • Chen, D.; Wang, Z.; Li, J.; Yang, Z.; Lin, L.; Liu, X.; Feng, X. Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Alkylidene Malonates: Highly Enantioselective Synthesis of Multisubstituted Isoxazolidines Chem.-Eur. J. 2011, 17, 5226 - 5229
    • (2011) Chem. - Eur. J. , vol.17 , pp. 5226-5229
    • Chen, D.1    Wang, Z.2    Li, J.3    Yang, Z.4    Lin, L.5    Liu, X.6    Feng, X.7
  • 42
    • 0037042276 scopus 로고    scopus 로고
    • Iron and Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Nitrones and Enals
    • Viton, F.; Bernardinelli, G.; Kündig, E. P. Iron and Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Nitrones and Enals J. Am. Chem. Soc. 2002, 124, 4968 - 4969
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 4968-4969
    • Viton, F.1    Bernardinelli, G.2    Kündig, E.P.3
  • 43
    • 54849407986 scopus 로고    scopus 로고
    • Iron- and Ruthenium-Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Enals and Diaryl Nitrones
    • Badoiu, A.; Bernardinelli, G.; Mareda, J.; Kündig, E. P.; Viton, F. Iron- And Ruthenium-Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Enals And Diaryl Nitrones Chem.-Asian J. 2008, 3, 1298 - 1311
    • (2008) Chem. - Asian J. , vol.3 , pp. 1298-1311
    • Badoiu, A.1    Bernardinelli, G.2    Mareda, J.3    Kündig, E.P.4    Viton, F.5
  • 44
    • 77953861133 scopus 로고    scopus 로고
    • Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloadditions between N-Methylnitrones and Enals
    • Badoiu, A.; Bernardinelli, G.; Kündig, E. P. Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloadditions between N-Methylnitrones and Enals Synthesis 2010, 2207 - 2212
    • (2010) Synthesis , pp. 2207-2212
    • Badoiu, A.1    Bernardinelli, G.2    Kündig, E.P.3
  • 45
    • 82955240876 scopus 로고    scopus 로고
    • Electronic Effects in 1,3-Dipolar Cycloaddition Reactions of N-Alkyl and N-Benzyl Nitrones with Dipolarophiles
    • Bdoiu, A.; Kündig, E. P. Electronic Effects in 1,3-Dipolar Cycloaddition Reactions of N-Alkyl And N-Benzyl Nitrones With Dipolarophiles Org. Biomol. Chem. 2012, 10, 114 - 121
    • (2012) Org. Biomol. Chem. , vol.10 , pp. 114-121
    • Bdoiu, A.1    Kündig, E.P.2
  • 46
    • 0001660873 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition of Nitrones Catalyzed by Optically Active Cationic Cobalt(III) Complexes
    • Mita, T.; Ohtsuki, N.; Ikeno, T.; Yamada, T. Enantioselective 1,3-Dipolar Cycloaddition of Nitrones Catalyzed by Optically Active Cationic Cobalt(III) Complexes Org. Lett. 2002, 4, 2457 - 2460
    • (2002) Org. Lett. , vol.4 , pp. 2457-2460
    • Mita, T.1    Ohtsuki, N.2    Ikeno, T.3    Yamada, T.4
  • 47
    • 0037560492 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition Reactions between Nitrones and α-Substituted α,β-Unsaturated Aldehydes Catalyzed by Chiral Cationic Cobalt(III) Complexes
    • Ohtsuki, N.; Kezuka, S.; Kogami, Y.; Mita, T.; Ashizawa, T.; Ikeno, T.; Yamada, T. Enantioselective 1,3-Dipolar Cycloaddition Reactions between Nitrones and α-Substituted α,β-Unsaturated Aldehydes Catalyzed by Chiral Cationic Cobalt(III) Complexes Synthesis 2003, 1462 - 1466
    • (2003) Synthesis , pp. 1462-1466
    • Ohtsuki, N.1    Kezuka, S.2    Kogami, Y.3    Mita, T.4    Ashizawa, T.5    Ikeno, T.6    Yamada, T.7
  • 48
    • 0345528016 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition Reaction of Nitrones with α,β-Unsaturated Aldehydes Catalyzed by Cationic 3-Oxobutylideneaminatocobalt(III) Complexes
    • Kezuka, S.; Ohtsuki, N.; Mita, T.; Kogami, Y.; Ashizawa, T.; Ikeno, T.; Yamada, T. Enantioselective 1,3-Dipolar Cycloaddition Reaction of Nitrones with α,β-Unsaturated Aldehydes Catalyzed by Cationic 3-Oxobutylideneaminatocobalt(III) Complexes Bull. Chem. Soc. Jpn. 2003, 76, 2197 - 2207
    • (2003) Bull. Chem. Soc. Jpn. , vol.76 , pp. 2197-2207
    • Kezuka, S.1    Ohtsuki, N.2    Mita, T.3    Kogami, Y.4    Ashizawa, T.5    Ikeno, T.6    Yamada, T.7
  • 49
    • 1642404440 scopus 로고    scopus 로고
    • Chiral DBFOX/Ph Complex Catalyzed Enantioselective Nitrone Cycloadditions to α,β-Unsaturated Aldehydes
    • Shirahase, M.; Kanemasa, S.; Oderaotoshi, Y. Chiral DBFOX/Ph Complex Catalyzed Enantioselective Nitrone Cycloadditions to α,β-Unsaturated Aldehydes Org. Lett. 2004, 6, 675 - 678
    • (2004) Org. Lett. , vol.6 , pp. 675-678
    • Shirahase, M.1    Kanemasa, S.2    Oderaotoshi, Y.3
  • 50
    • 2342652407 scopus 로고    scopus 로고
    • Improved Catalysis of Nitrone 1,3-Dipolar Cycloadditions by Solving the Aggregation Issue of the DBFOX/Ph-Transition Metal Complexes
    • Shirahase, M.; Kanemasa, S.; Hasegawa, M. Improved Catalysis of Nitrone 1,3-Dipolar Cycloadditions by Solving the Aggregation Issue of the DBFOX/Ph-Transition Metal Complexes Tetrahedron Lett. 2004, 45, 4061 - 4063
    • (2004) Tetrahedron Lett. , vol.45 , pp. 4061-4063
    • Shirahase, M.1    Kanemasa, S.2    Hasegawa, M.3
  • 51
    • 12144286166 scopus 로고    scopus 로고
    • The Complete Characterization of a Rhodium Lewis Acid-Dipolarophile Complex as an Intermediate for the Enantioselective Catalytic 1,3-Dipolar Cycloaddition of C,N-Diphenylnitrone to Methacrolein
    • Carmona, D.; Lamata, M. P.; Viguri, F.; Rodríguez, R.; Oro, L. A.; Balana, A. I.; Lahoz, F. J.; Tejero, T.; Merino, P.; Franco, S.; Montesa, I. The Complete Characterization of a Rhodium Lewis Acid-Dipolarophile Complex as an Intermediate for the Enantioselective Catalytic 1,3-Dipolar Cycloaddition of C,N-Diphenylnitrone to Methacrolein J. Am. Chem. Soc. 2004, 126, 2716 - 2717
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 2716-2717
    • Carmona, D.1    Lamata, M.P.2    Viguri, F.3    Rodríguez, R.4    Oro, L.A.5    Balana, A.I.6    Lahoz, F.J.7    Tejero, T.8    Merino, P.9    Franco, S.10    Montesa, I.11
  • 53
    • 33748688215 scopus 로고    scopus 로고
    • Chiral Half-Sandwich Ruthenium(II) Complexes as Catalysts in 1,3-Dipolar Cycloaddition Reactions of Nitrones with Methacrolein
    • Carmona, D.; Lamata, M. P.; Viguri, F.; Ferrer, J.; García, N.; Lahoz, F. J.; Martín, M. L.; Oro, L. A. Chiral Half-Sandwich Ruthenium(II) Complexes as Catalysts in 1,3-Dipolar Cycloaddition Reactions of Nitrones with Methacrolein Eur. J. Inorg. Chem. 2006, 3155 - 3166
    • (2006) Eur. J. Inorg. Chem. , pp. 3155-3166
    • Carmona, D.1    Lamata, M.P.2    Viguri, F.3    Ferrer, J.4    García, N.5    Lahoz, F.J.6    Martín, M.L.7    Oro, L.A.8
  • 54
    • 34547184971 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition Reaction between α,β-Unsaturated Aldehydes and Nitrones Catalyzed by Well-Defined Iridium or Rhodium Catalysts
    • Carmona, D.; Lamata, M. P.; Viguri, F.; Rodríguez, R.; Fischer, T.; Lahoz, F. J.; Dobrinovitch, I. T.; Oro, L. A. Asymmetric 1,3-Dipolar Cycloaddition Reaction between α,β-Unsaturated Aldehydes And Nitrones Catalyzed by Well-Defined Iridium or Rhodium Catalysts Adv. Synth. Catal. 2007, 349, 1751 - 1758
    • (2007) Adv. Synth. Catal. , vol.349 , pp. 1751-1758
    • Carmona, D.1    Lamata, M.P.2    Viguri, F.3    Rodríguez, R.4    Fischer, T.5    Lahoz, F.J.6    Dobrinovitch, I.T.7    Oro, L.A.8
  • 55
    • 84875445349 scopus 로고    scopus 로고
    • Chiral Octahedral Phosphano-Oxazoline Iridium(III) Complexes as Catalysts in Asymmetric Cycloaddition Reactions
    • Carmona, D.; Ferrer, J.; García, N.; Ramírez, P.; Lahoz, F. J.; García-Orduña, P.; Oro, L. A. Chiral Octahedral Phosphano-Oxazoline Iridium(III) Complexes as Catalysts in Asymmetric Cycloaddition Reactions Organometallics 2013, 32, 1609 - 1619
    • (2013) Organometallics , vol.32 , pp. 1609-1619
    • Carmona, D.1    Ferrer, J.2    García, N.3    Ramírez, P.4    Lahoz, F.J.5    García-Orduña, P.6    Oro, L.A.7
  • 56
    • 39849087916 scopus 로고    scopus 로고
    • Cationic Chiral Dirhodium Carboxamidates Are Activated for Lewis Acid Catalysis
    • Wang, Y.; Wolf, J.; Zavalij, P.; Doyle, M. P. Cationic Chiral Dirhodium Carboxamidates Are Activated for Lewis Acid Catalysis Angew. Chem., Int. Ed. 2008, 47, 1439 - 1442
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 1439-1442
    • Wang, Y.1    Wolf, J.2    Zavalij, P.3    Doyle, M.P.4
  • 57
    • 79959187553 scopus 로고    scopus 로고
    • Solvent Enhancement of Reaction Selectivity: A Unique Property of Cationic Chiral Dirhodium Carboxamidates
    • Wang, X.; Weigl, C.; Doyle, M. P. Solvent Enhancement of Reaction Selectivity: A Unique Property of Cationic Chiral Dirhodium Carboxamidates J. Am. Chem. Soc. 2011, 133, 9572 - 9579
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 9572-9579
    • Wang, X.1    Weigl, C.2    Doyle, M.P.3
  • 58
    • 24144446123 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition Reaction of Nitrones and Acrolein with a Bis-Titanium Catalyst as Chiral Lewis Acid
    • Kano, T.; Hashimoto, T.; Maruoka, K. Asymmetric 1,3-Dipolar Cycloaddition Reaction of Nitrones and Acrolein with a Bis-Titanium Catalyst as Chiral Lewis Acid J. Am. Chem. Soc. 2005, 127, 11926 - 11927
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 11926-11927
    • Kano, T.1    Hashimoto, T.2    Maruoka, K.3
  • 59
    • 36349023884 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloadditions of Nitrones and Methacrolein Catalyzed by Chiral Bis-Titanium Lewis Acid: A Dramatic Effect of N-Substituent on Nitrone
    • Hashimoto, T.; Omote, M.; Kano, T.; Maruoka, K. Asymmetric 1,3-Dipolar Cycloadditions of Nitrones and Methacrolein Catalyzed by Chiral Bis-Titanium Lewis Acid: A Dramatic Effect of N-Substituent on Nitrone Org. Lett. 2007, 9, 4805 - 4808
    • (2007) Org. Lett. , vol.9 , pp. 4805-4808
    • Hashimoto, T.1    Omote, M.2    Kano, T.3    Maruoka, K.4
  • 60
    • 45449090601 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloadditions of N-Benzyl and N-Diphenylmethyl Nitrones and α,β-Unsaturated Aldehydes Catalyzed by Bis-Titanium Chiral Lewis Acids
    • Hashimoto, T.; Omote, M.; Hato, Y.; Kano, T.; Maruoka, K. Asymmetric 1,3-Dipolar Cycloadditions of N-Benzyl and N-Diphenylmethyl Nitrones and α,β-Unsaturated Aldehydes Catalyzed by Bis-Titanium Chiral Lewis Acids Chem.-Asian J. 2008, 3, 407 - 412
    • (2008) Chem. - Asian J. , vol.3 , pp. 407-412
    • Hashimoto, T.1    Omote, M.2    Hato, Y.3    Kano, T.4    Maruoka, K.5
  • 61
    • 45449093805 scopus 로고    scopus 로고
    • 6,6′-Substituent Effect of BINOL in Bis-Titanium Chiral Lewis Acid Catalyzed 1,3-Dipolar Cycloaddition of Nitrones
    • Hashimoto, T.; Omote, M.; Maruoka, K. 6,6′-Substituent Effect of BINOL in Bis-Titanium Chiral Lewis Acid Catalyzed 1,3-Dipolar Cycloaddition of Nitrones Org. Biomol. Chem. 2008, 6, 2263 - 2265
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 2263-2265
    • Hashimoto, T.1    Omote, M.2    Maruoka, K.3
  • 62
    • 84898955926 scopus 로고    scopus 로고
    • Enantioselective Ruthenium-Catalyzed 1,3-Dipolar Cycloadditions between C-Carboalkoxy Ketonitrones and Methacrolein: Solvent Effect on Reaction Selectivity and Its Rational
    • Selim, K. B.; Martel, A.; Laurent, M. Y.; Lhoste, J.; Py, S.; Dujardin, G. Enantioselective Ruthenium-Catalyzed 1,3-Dipolar Cycloadditions between C-Carboalkoxy Ketonitrones and Methacrolein: Solvent Effect on Reaction Selectivity and Its Rational J. Org. Chem. 2014, 79, 3414 - 3426
    • (2014) J. Org. Chem. , vol.79 , pp. 3414-3426
    • Selim, K.B.1    Martel, A.2    Laurent, M.Y.3    Lhoste, J.4    Py, S.5    Dujardin, G.6
  • 63
    • 37249031974 scopus 로고    scopus 로고
    • Half-Sandwich Rhodium (and Iridium) Complexes as Enantioselective Catalysts for the 1,3-Dipolar Cycloaddition of 3,4-Dihydroisoquinoline N-Oxide to Methacrylonitrile
    • Carmona, D.; Lamata, M. P.; Viguri, F.; Rodríguez, R.; Lahoz, F. J.; Oro, L. A. Half-Sandwich Rhodium (and Iridium) Complexes as Enantioselective Catalysts for the 1,3-Dipolar Cycloaddition of 3,4-Dihydroisoquinoline N-Oxide to Methacrylonitrile Chem.-Eur. J. 2007, 13, 9746 - 9756
    • (2007) Chem. - Eur. J. , vol.13 , pp. 9746-9756
    • Carmona, D.1    Lamata, M.P.2    Viguri, F.3    Rodríguez, R.4    Lahoz, F.J.5    Oro, L.A.6
  • 64
    • 66149162957 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition Reaction of α,β-Unsaturated Nitriles with Nitrones Catalyzed by Chiral-at-Metal Rhodium or Iridium Complexes
    • Carmona, D.; Lamata, M. P.; Viguri, F.; Rodríguez, R.; Lahoz, F. J.; Fabra, M. J.; Oro, L. A. Asymmetric 1,3-Dipolar Cycloaddition Reaction of α,β-Unsaturated Nitriles with Nitrones Catalyzed by Chiral-at-Metal Rhodium or Iridium Complexes Tetrahedron: Asymmetry 2009, 20, 1197 - 1205
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1197-1205
    • Carmona, D.1    Lamata, M.P.2    Viguri, F.3    Rodríguez, R.4    Lahoz, F.J.5    Fabra, M.J.6    Oro, L.A.7
  • 65
    • 78649747850 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Nitrones with Propioloylpyrazoles and Acryloylpyrazoles Induced by Chiral π-Cation Catalysts
    • Sakakura, A.; Hori, M.; Fushimi, M.; Ishihara, K. Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Nitrones with Propioloylpyrazoles And Acryloylpyrazoles Induced by Chiral π-Cation Catalysts J. Am. Chem. Soc. 2010, 132, 15550 - 15552
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 15550-15552
    • Sakakura, A.1    Hori, M.2    Fushimi, M.3    Ishihara, K.4
  • 66
    • 84986584131 scopus 로고    scopus 로고
    • Regio- and Enantioselective Nitrone Cycloaddition to Alkynones for the Synthesis of Δ4-Isoxazolines
    • Sibi, M. P.; Dunkle, K. L.; Rane, D. Regio- And Enantioselective Nitrone Cycloaddition to Alkynones for the Synthesis of Δ4-Isoxazolines Heterocycles 2014, 88, 1639 - 1647
    • (2014) Heterocycles , vol.88 , pp. 1639-1647
    • Sibi, M.P.1    Dunkle, K.L.2    Rane, D.3
  • 67
    • 84877252396 scopus 로고    scopus 로고
    • Gold Catalyzed Enantioselective Intermolecular [3 + 2] Dipolar Cycloaddition of N-Allenyl Amides with Nitrones
    • Li, G. H.; Zhou, W.; Li, X. X.; Bi, Q. W.; Wang, Z.; Zhao, Z. G.; Hu, W. X.; Chen, Z. Gold Catalyzed Enantioselective Intermolecular [3 + 2] Dipolar Cycloaddition of N-Allenyl Amides with Nitrones Chem. Commun. 2013, 49, 4770 - 4772
    • (2013) Chem. Commun. , vol.49 , pp. 4770-4772
    • Li, G.H.1    Zhou, W.2    Li, X.X.3    Bi, Q.W.4    Wang, Z.5    Zhao, Z.G.6    Hu, W.X.7    Chen, Z.8
  • 68
    • 0028361611 scopus 로고
    • Asymmetric 13-Dipolar Cycloaddition of Nitrones with Ketene Acetals Catalyzed by Chiral Oxazaborolidines
    • Seerden, J.-P. G.; Scholte op Reimer, A. W. A.; Scheeren, H. W. Asymmetric 13-Dipolar Cycloaddition of Nitrones with Ketene Acetals Catalyzed by Chiral Oxazaborolidines Tetrahedron Lett. 1994, 35, 4419 - 4422
    • (1994) Tetrahedron Lett. , vol.35 , pp. 4419-4422
    • Seerden, J.-P.G.1    Scholte Op Reimer, A.W.A.2    Scheeren, H.W.3
  • 69
    • 0029033931 scopus 로고
    • Dramatic Solvents Effects on the Enantioselectivity of Chiral Oxazaborolidine Catalyzed Asymmetric 1,3-Dipolar Cycloadditions of Nitrones with Ketene Acetals
    • Seerden, J.-P. G.; Scholte op Reimer, A. W. A.; Scheeren, H. W. Dramatic Solvents Effects on the Enantioselectivity of Chiral Oxazaborolidine Catalyzed Asymmetric 1,3-Dipolar Cycloadditions of Nitrones with Ketene Acetals Tetrahedron: Asymmetry 1995, 6, 1441 - 1450
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 1441-1450
    • Seerden, J.-P.G.1    Scholte Op Reimer, A.W.A.2    Scheeren, H.W.3
  • 70
    • 0030877158 scopus 로고    scopus 로고
    • 1,3-Dipolar Cycloaddition Reactions of Nitrones with Alkyl Vinyl Ethers Catalyzed by Chiral Oxazaborolidines
    • Seerden, J.-P. G.; Boeren, M. M. M.; Scheeren, H. W. 1,3-Dipolar Cycloaddition Reactions of Nitrones with Alkyl Vinyl Ethers Catalyzed by Chiral Oxazaborolidines Tetrahedron 1997, 53, 11843 - 11852
    • (1997) Tetrahedron , vol.53 , pp. 11843-11852
    • Seerden, J.-P.G.1    Boeren, M.M.M.2    Scheeren, H.W.3
  • 71
    • 0033611996 scopus 로고    scopus 로고
    • Catalytic Enantioselective Inverse-Electron Demand 1,3-Dipolar Cycloaddition Reactions of Nitrones with Alkenes
    • Simonsen, K. B.; Bayón, P.; Hazell, R. G.; Gothelf, K. V.; Jorgensen, K. A. Catalytic Enantioselective Inverse-Electron Demand 1,3-Dipolar Cycloaddition Reactions of Nitrones with Alkenes J. Am. Chem. Soc. 1999, 121, 3845 - 3853
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 3845-3853
    • Simonsen, K.B.1    Bayón, P.2    Hazell, R.G.3    Gothelf, K.V.4    Jorgensen, K.A.5
  • 72
    • 0034731588 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloaddition Reactions of Cyclic Nitrones: A Simple Approach for the Formation of Optically Active Isoquinoline Derivatives
    • Jensen, K. B.; Roberson, M.; Jorgensen, K. A. Catalytic Enantioselective 1,3-Dipolar Cycloaddition Reactions of Cyclic Nitrones: A Simple Approach for the Formation of Optically Active Isoquinoline Derivatives J. Org. Chem. 2000, 65, 9080 - 9084
    • (2000) J. Org. Chem. , vol.65 , pp. 9080-9084
    • Jensen, K.B.1    Roberson, M.2    Jorgensen, K.A.3
  • 73
    • 0033532033 scopus 로고    scopus 로고
    • The First Highly Diastereo- and Enantioselective Polymeric Catalyst for the 1,3-Cycloaddition Reaction of Nitrones with Alkenes
    • Simonsen, K. B.; Jorgensen, K. A.; Hu, Q.-S.; Pu, L. The First Highly Diastereo- and Enantioselective Polymeric Catalyst for the 1,3-Cycloaddition Reaction of Nitrones with Alkenes Chem. Commun. 1999, 811 - 8112
    • (1999) Chem. Commun. , pp. 811-8112
    • Simonsen, K.B.1    Jorgensen, K.A.2    Hu, Q.-S.3    Pu, L.4
  • 74
    • 0033515568 scopus 로고    scopus 로고
    • Copper(II)-Bisoxazoline Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions of Nitrones with Electron-Rich Alkenes
    • Jensen, K. B.; Hazell, R. G.; Jorgensen, K. A. Copper(II)-Bisoxazoline Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions of Nitrones with Electron-Rich Alkenes J. Org. Chem. 1999, 64, 2353 - 2360
    • (1999) J. Org. Chem. , vol.64 , pp. 2353-2360
    • Jensen, K.B.1    Hazell, R.G.2    Jorgensen, K.A.3
  • 75
    • 0034608075 scopus 로고    scopus 로고
    • Use of Chiral Ti(IV) Complexes in the Cycloaddition of C,N-Diphenylnitrone to tert -Butyl Vinyl Ether
    • Bayón, P.; de March, P.; Espinosa, M.; Figueredo, M.; Font, J. Use of Chiral Ti(IV) Complexes in the Cycloaddition of C,N-Diphenylnitrone to tert -Butyl Vinyl Ether Tetrahedron: Asymmetry 2000, 11, 1757 - 1765
    • (2000) Tetrahedron: Asymmetry , vol.11 , pp. 1757-1765
    • Bayón, P.1    De March, P.2    Espinosa, M.3    Figueredo, M.4    Font, J.5
  • 76
    • 0034601961 scopus 로고    scopus 로고
    • Use of Chiral B(III) Complexes in the Cycloaddition of C,N-Diphenylnitrone to tert -Butyl Vinyl Ether
    • Bayón, P.; de March, P.; Figueredo, M.; Font, J.; Medrano, J. Use of Chiral B(III) Complexes in the Cycloaddition of C,N-Diphenylnitrone to tert -Butyl Vinyl Ether Tetrahedron: Asymmetry 2000, 11, 4269 - 4278
    • (2000) Tetrahedron: Asymmetry , vol.11 , pp. 4269-4278
    • Bayón, P.1    De March, P.2    Figueredo, M.3    Font, J.4    Medrano, J.5
  • 77
    • 0034784173 scopus 로고    scopus 로고
    • Tetranuclear Titanium 7,7′-Modified Binaphtholate Cluster as a Novel Chiral Lewis Acid Catalyst
    • Mikami, K.; Ueki, M.; Matsumoto, Y.; Terada, M. Tetranuclear Titanium 7,7′-Modified Binaphtholate Cluster as a Novel Chiral Lewis Acid Catalyst Chirality 2001, 13, 541 - 544
    • (2001) Chirality , vol.13 , pp. 541-544
    • Mikami, K.1    Ueki, M.2    Matsumoto, Y.3    Terada, M.4
  • 78
    • 0032532791 scopus 로고    scopus 로고
    • Palladium(II)-Catalyzed 1,3-Dipolar Cycloaddition of Nitrones with Enol Ethers
    • Hori, K.; Itoh, J.; Ohta, T.; Furukawa, I. Palladium(II)-Catalyzed 1,3-Dipolar Cycloaddition of Nitrones with Enol Ethers Tetrahedron 1998, 54, 12737 - 12744
    • (1998) Tetrahedron , vol.54 , pp. 12737-12744
    • Hori, K.1    Itoh, J.2    Ohta, T.3    Furukawa, I.4
  • 79
    • 33751250813 scopus 로고    scopus 로고
    • Endo-Selective Asymmetric Inverse Electron-Demand 1,3-Dipolar Cycloaddition Reaction of Nitrones
    • Ashizawa, T.; Ohtsuki, N.; Miura, T.; Ohya, M.; Shinozaki, T.; Ikeno, T.; Yamada, T. Endo-Selective Asymmetric Inverse Electron-Demand 1,3-Dipolar Cycloaddition Reaction of Nitrones Heterocycles 2006, 68, 1801 - 1810
    • (2006) Heterocycles , vol.68 , pp. 1801-1810
    • Ashizawa, T.1    Ohtsuki, N.2    Miura, T.3    Ohya, M.4    Shinozaki, T.5    Ikeno, T.6    Yamada, T.7
  • 80
    • 84655162188 scopus 로고    scopus 로고
    • Catalytic Asymmetric Cycloaddition Reaction of Alkenyl Trichloroacetates with Nitrones
    • Yanagisawa, A.; Izumiseki, A.; Sugita, T.; Kushihara, N.; Yoshida, K. Catalytic Asymmetric Cycloaddition Reaction of Alkenyl Trichloroacetates with Nitrones Synlett 2012, 107 - 112
    • (2012) Synlett , pp. 107-112
    • Yanagisawa, A.1    Izumiseki, A.2    Sugita, T.3    Kushihara, N.4    Yoshida, K.5
  • 81
    • 0031496734 scopus 로고    scopus 로고
    • Enantio- and Diastereoselective Synthesis of Isoxazolidines by Asymmetric 1,3-Dipolar Cycloaddition of Nitrones
    • Ukaji, Y.; Taniguchi, K.; Sada, K.; Inomata, K. Enantio- and Diastereoselective Synthesis of Isoxazolidines by Asymmetric 1,3-Dipolar Cycloaddition of Nitrones Chem. Lett. 1997, 26, 547 - 548
    • (1997) Chem. Lett. , vol.26 , pp. 547-548
    • Ukaji, Y.1    Taniguchi, K.2    Sada, K.3    Inomata, K.4
  • 82
    • 0035533876 scopus 로고    scopus 로고
    • A Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Allyl Alcohol
    • Ding, X.; Taniguchi, K.; Ukaji, Y.; Inomata, K. A Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Allyl Alcohol Chem. Lett. 2001, 30, 468 - 469
    • (2001) Chem. Lett. , vol.30 , pp. 468-469
    • Ding, X.1    Taniguchi, K.2    Ukaji, Y.3    Inomata, K.4
  • 83
    • 0036012075 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar Cycloaddition of a Nitrone Bearing a Bulky Amide Moiety to γ-Substituted Allylic Alcohols
    • Ding, X.; Ukaji, Y.; Fujinami, S.; Inomata, K. Catalytic Asymmetric 1,3-Dipolar Cycloaddition of a Nitrone Bearing a Bulky Amide Moiety to γ-Substituted Allylic Alcohols Chem. Lett. 2002, 31, 302 - 303
    • (2002) Chem. Lett. , vol.31 , pp. 302-303
    • Ding, X.1    Ukaji, Y.2    Fujinami, S.3    Inomata, K.4
  • 84
    • 33750576560 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition of Nitrones with an Electron-Withdrawing Group to Allylic Alcohols Utilizing Diisopropyl Tartrate as a Chiral Auxiliary
    • Ding, X.; Taniguchi, K.; Hamamoto, Y.; Sada, K.; Fujinami, S.; Ukaji, Y.; Inomata, K. Asymmetric 1,3-Dipolar Cycloaddition of Nitrones with an Electron-Withdrawing Group to Allylic Alcohols Utilizing Diisopropyl Tartrate as a Chiral Auxiliary Bull. Chem. Soc. Jpn. 2006, 79, 1069 - 1083
    • (2006) Bull. Chem. Soc. Jpn. , vol.79 , pp. 1069-1083
    • Ding, X.1    Taniguchi, K.2    Hamamoto, Y.3    Sada, K.4    Fujinami, S.5    Ukaji, Y.6    Inomata, K.7
  • 85
    • 77953681714 scopus 로고    scopus 로고
    • 1,3-Dipolar Cycloaddition Reactions Catalyzed by Heterocycle-Based Metal Complexes
    • Ukaji, Y.; Inomata, K. 1,3-Dipolar Cycloaddition Reactions Catalyzed By Heterocycle-Based Metal Complexes Chem. Rec. 2010, 10, 173 - 187
    • (2010) Chem. Rec. , vol.10 , pp. 173-187
    • Ukaji, Y.1    Inomata, K.2
  • 86
    • 0034638388 scopus 로고    scopus 로고
    • New Strategies for Organic Catalysis: The First Enantioselective Organocatalytic 1,3-Dipolar Cycloaddition
    • Jen, W. S.; Wiener, J. J. M.; MacMillan, D. W. C. New Strategies for Organic Catalysis: The First Enantioselective Organocatalytic 1,3-Dipolar Cycloaddition J. Am. Chem. Soc. 2000, 122, 9874 - 9875
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9874-9875
    • Jen, W.S.1    Wiener, J.J.M.2    MacMillan, D.W.C.3
  • 87
    • 1242286035 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloadditions of Unsaturated Aldehydes Promoted by A Poly(ethylene glycol)-Supported Organic Catalyst
    • Puglisi, A.; Benaglia, M.; Cinquini, M.; Cozzi, F.; Celentano, G. Enantioselective 1,3-Dipolar Cycloadditions of Unsaturated Aldehydes Promoted by A Poly(ethylene glycol)-Supported Organic Catalyst Eur. J. Org. Chem. 2004, 567 - 573
    • (2004) Eur. J. Org. Chem. , pp. 567-573
    • Puglisi, A.1    Benaglia, M.2    Cinquini, M.3    Cozzi, F.4    Celentano, G.5
  • 88
    • 85033415210 scopus 로고    scopus 로고
    • Synthesis and Application of a Recyclable Ionic Liquid-Supported Imidazolidinone Catalyst in Enantioselective 1,3-Dipolar Cycloaddition
    • Shen, Z.-L.; Goh, K. K. K.; Wong, C. H. A.; Loo, W.-Y.; Yang, Y.-S.; Lu, J.; Loh, T.-P. Synthesis and Application of a Recyclable Ionic Liquid-Supported Imidazolidinone Catalyst in Enantioselective 1,3-Dipolar Cycloaddition Chem. Commun. 2012, 48, 5856 - 5858
    • (2012) Chem. Commun. , vol.48 , pp. 5856-5858
    • Shen, Z.-L.1    Goh, K.K.K.2    Wong, C.H.A.3    Loo, W.-Y.4    Yang, Y.-S.5    Lu, J.6    Loh, T.-P.7
  • 89
    • 84890586356 scopus 로고    scopus 로고
    • A Magnetoclick Imidazolidinone Nanocatalyst for Asymmetric 1,3-Dipolar Cycloadditions
    • Pagoti, S.; Dutta, D.; Dash, J. A Magnetoclick Imidazolidinone Nanocatalyst for Asymmetric 1,3-Dipolar Cycloadditions Adv. Synth. Catal. 2013, 355, 3532 - 3538
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 3532-3538
    • Pagoti, S.1    Dutta, D.2    Dash, J.3
  • 90
    • 84903834195 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloadditions of Nitrones with Unsaturated Aldehydes Promoted by a Recyclable Tetraarylphosphonium Supported Imidazolidinone Catalyst
    • Nie, X.; Lu, C.; Chen, Z.; Yang, G.; Nie, J. Enantioselective 1,3-Dipolar Cycloadditions of Nitrones with Unsaturated Aldehydes Promoted by a Recyclable Tetraarylphosphonium Supported Imidazolidinone Catalyst J. Mol. Catal. A: Chem. 2014, 393, 171 - 174
    • (2014) J. Mol. Catal. A: Chem. , vol.393 , pp. 171-174
    • Nie, X.1    Lu, C.2    Chen, Z.3    Yang, G.4    Nie, J.5
  • 91
    • 0037166699 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloaddition of Nitrones to Cyclopent-1-enecarbaldehyde
    • Karlsson, S.; Högberg, H.-E. Catalytic Enantioselective 1,3-Dipolar Cycloaddition of Nitrones to Cyclopent-1-enecarbaldehyde Tetrahedron: Asymmetry 2002, 13, 923 - 926
    • (2002) Tetrahedron: Asymmetry , vol.13 , pp. 923-926
    • Karlsson, S.1    Högberg, H.-E.2
  • 92
    • 0043157645 scopus 로고    scopus 로고
    • Organocatalysts Promote Enantioselective 1,3-Dipolar Cycloadditions of Nitrones with 1-Cycloalkene-1-carboxaldehydes
    • Karlsson, S.; Högberg, H.-E. Organocatalysts Promote Enantioselective 1,3-Dipolar Cycloadditions of Nitrones with 1-Cycloalkene-1-carboxaldehydes Eur. J. Org. Chem. 2003, 2782 - 2791
    • (2003) Eur. J. Org. Chem. , pp. 2782-2791
    • Karlsson, S.1    Högberg, H.-E.2
  • 93
    • 33845192393 scopus 로고    scopus 로고
    • A New Organocatalyst for 1,3-Dipolar Cycloadditions of Nitrones to α,β-Unsaturated Aldehydes
    • Chow, S. S.; Nevalainen, M.; Evans, C. A.; Johannes, C. W. A New Organocatalyst for 1,3-Dipolar Cycloadditions of Nitrones to α,β-Unsaturated Aldehydes Tetrahedron Lett. 2007, 48, 277 - 280
    • (2007) Tetrahedron Lett. , vol.48 , pp. 277-280
    • Chow, S.S.1    Nevalainen, M.2    Evans, C.A.3    Johannes, C.W.4
  • 94
    • 34447268984 scopus 로고    scopus 로고
    • A Simple One-Pot, Three-Component, Catalytic, Highly Enantioselective Isoxazolidine Synthesis
    • Rios, R.; Ibrahem, I.; Vesely, J.; Zhao, G.-L.; Córdova, A. A Simple One-Pot, Three-Component, Catalytic, Highly Enantioselective Isoxazolidine Synthesis Tetrahedron Lett. 2007, 48, 5701 - 5705
    • (2007) Tetrahedron Lett. , vol.48 , pp. 5701-5705
    • Rios, R.1    Ibrahem, I.2    Vesely, J.3    Zhao, G.-L.4    Córdova, A.5
  • 96
    • 69249089792 scopus 로고    scopus 로고
    • Hybrid Diamines Derived from 1,1′-Binaphthyl-2,2′-Diamine and α-Amino Acids as Organocatalysts for 1,3-Dipolar Cycloaddition of Aromatic Nitrones to (E)-Crotonaldehyde
    • Weselinski, L.; Stepniak, P.; Jurczak, J. Hybrid Diamines Derived from 1,1′-Binaphthyl-2,2′-Diamine and α-Amino Acids as Organocatalysts for 1,3-Dipolar Cycloaddition of Aromatic Nitrones to (E)-Crotonaldehyde Synlett 2009, 2261 - 2264
    • (2009) Synlett , pp. 2261-2264
    • Weselinski, L.1    Stepniak, P.2    Jurczak, J.3
  • 97
    • 34948875227 scopus 로고    scopus 로고
    • Hydrazide-Catalyzed 1,3-Dipolar Nitrone Cycloadditions
    • Lemay, M.; Trant, J.; Ogilvie, W. W. Hydrazide-Catalyzed 1,3-Dipolar Nitrone Cycloadditions Tetrahedron 2007, 63, 11644 - 11655
    • (2007) Tetrahedron , vol.63 , pp. 11644-11655
    • Lemay, M.1    Trant, J.2    Ogilvie, W.W.3
  • 98
    • 78650231701 scopus 로고    scopus 로고
    • The Highly Enantioselective 1,3-Dipolar Cycloaddition of Alkyl Glyoxylate-Derived Nitrones to E-Crotonaldehyde Catalyzed by Hybrid Diamines
    • Weseliński, L.; Słyk, E.; Jurczak, J. The Highly Enantioselective 1,3-Dipolar Cycloaddition of Alkyl Glyoxylate-Derived Nitrones to E-Crotonaldehyde Catalyzed by Hybrid Diamines Tetrahedron Lett. 2011, 52, 381 - 384
    • (2011) Tetrahedron Lett. , vol.52 , pp. 381-384
    • Weseliński, L.1    Słyk, E.2    Jurczak, J.3
  • 99
    • 84859377996 scopus 로고    scopus 로고
    • The Asymmetric Organocatalytic 1,3-Dipolar Cycloaddition of Alkyl Pyruvate-Derived Nitrones and α,β-Unsaturated Aldehydes
    • Weseliński; Kalinowska, E.; Jurczak, J. The Asymmetric Organocatalytic 1,3-Dipolar Cycloaddition of Alkyl Pyruvate-Derived Nitrones and α,β-Unsaturated Aldehydes Tetrahedron: Asymmetry 2012, 23, 264 - 270
    • (2012) Tetrahedron: Asymmetry , vol.23 , pp. 264-270
    • Weseliński1    Kalinowska, E.2    Jurczak, J.3
  • 100
    • 84870693002 scopus 로고    scopus 로고
    • Organocatalytic Enantio- and Diastereoselective 1,3-Dipolar Cycloaddition between Alanine-Derived Ketonitrones and e -Crotonaldehyde: Efficiency and Full Stereochemical Studies
    • Selim, K. B.; Beauchard, A.; Lhoste, J.; Martel, A.; Laurent, M. Y.; Dujardin, G. Organocatalytic Enantio- and Diastereoselective 1,3-Dipolar Cycloaddition between Alanine-Derived Ketonitrones and E -Crotonaldehyde: Efficiency and Full Stereochemical Studies Tetrahedron: Asymmetry 2012, 23, 1670 - 1677
    • (2012) Tetrahedron: Asymmetry , vol.23 , pp. 1670-1677
    • Selim, K.B.1    Beauchard, A.2    Lhoste, J.3    Martel, A.4    Laurent, M.Y.5    Dujardin, G.6
  • 101
    • 70349753180 scopus 로고    scopus 로고
    • Nine-Step Enantioselective Total Synthesis of (+)-Minfiensine
    • Jones, S. B.; Simmons, B.; MacMillan, D. W. C. Nine-Step Enantioselective Total Synthesis of (+)-Minfiensine J. Am. Chem. Soc. 2009, 131, 13606 - 13607
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 13606-13607
    • Jones, S.B.1    Simmons, B.2    MacMillan, D.W.C.3
  • 102
    • 84863115934 scopus 로고    scopus 로고
    • Organocatalytic Enantioselective Dipolar [3 + 2] Cycloadditions of Acetylenic Aldehydes with Nitrones for the Formation of Chiral 4-Isoxazolines
    • Cai, X.; Wang, C.; Sun, J. Organocatalytic Enantioselective Dipolar [3 + 2] Cycloadditions of Acetylenic Aldehydes with Nitrones for the Formation of Chiral 4-Isoxazolines Adv. Synth. Catal. 2012, 354, 359 - 363
    • (2012) Adv. Synth. Catal. , vol.354 , pp. 359-363
    • Cai, X.1    Wang, C.2    Sun, J.3
  • 103
    • 84862540451 scopus 로고    scopus 로고
    • Enantioselective Synthesis of 4-Isoxazolines by 1,3-Dipolar Cycloadditions of Nitrones to Alkynals Catalyzed by Fluorodiphenylmethylpyrrolidines
    • Alemán, J.; Fraile, A.; Marzo, L.; Ruano, J. L. G.; Izquierdo, C.; Díaz-Tendero, S. Enantioselective Synthesis of 4-Isoxazolines by 1,3-Dipolar Cycloadditions of Nitrones to Alkynals Catalyzed by Fluorodiphenylmethylpyrrolidines Adv. Synth. Catal. 2012, 354, 1665 - 1671
    • (2012) Adv. Synth. Catal. , vol.354 , pp. 1665-1671
    • Alemán, J.1    Fraile, A.2    Marzo, L.3    Ruano, J.L.G.4    Izquierdo, C.5    Díaz-Tendero, S.6
  • 104
    • 0037455338 scopus 로고    scopus 로고
    • Metal-Free, Noncovalent Catalysis of Diels-Alder Reactions by Neutral Hydrogen Bond Donors in Organic Solvents and in Water
    • Wittkopp, A.; Schreiner, P. R. Metal-Free, Noncovalent Catalysis of Diels-Alder Reactions by Neutral Hydrogen Bond Donors in Organic Solvents and in Water Chem.-Eur. J. 2003, 9, 407 - 414
    • (2003) Chem. - Eur. J. , vol.9 , pp. 407-414
    • Wittkopp, A.1    Schreiner, P.R.2
  • 105
    • 57649134975 scopus 로고    scopus 로고
    • Organocatalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Nitroolefins
    • Du, W.; Liu, Y. K.; Yue, L.; Chen, Y. C. Organocatalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Nitroolefins Synlett 2008, 2997 - 3000
    • (2008) Synlett , pp. 2997-3000
    • Du, W.1    Liu, Y.K.2    Yue, L.3    Chen, Y.C.4
  • 106
    • 4344713238 scopus 로고    scopus 로고
    • Highly Enantioselective Catalytic Acyl-Pictet-Spengler Reactions
    • Taylor, M. S.; Jacobsen, E. N. Highly Enantioselective Catalytic Acyl-Pictet-Spengler Reactions J. Am. Chem. Soc. 2004, 126, 10558 - 10559
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 10558-10559
    • Taylor, M.S.1    Jacobsen, E.N.2
  • 107
    • 53249085441 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition of Nitrones with Ethyl Vinyl Ether: The Difference between Bronsted and Lewis Acid Catalysis
    • Jiao, P.; Nakashima, D.; Yamamoto, H. Enantioselective 1,3-Dipolar Cycloaddition of Nitrones with Ethyl Vinyl Ether: The Difference Between Bronsted and Lewis Acid Catalysis Angew. Chem., Int. Ed. 2008, 47, 2411 - 2413
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 2411-2413
    • Jiao, P.1    Nakashima, D.2    Yamamoto, H.3
  • 108
    • 37049125041 scopus 로고
    • The Reactions of Copper(I) Phenylacetylide with Nitrones
    • Kinugasa, M.; Hashimoto, S. The Reactions of Copper(I) Phenylacetylide with Nitrones J. Chem. Soc., Chem. Commun. 1972, 466 - 467
    • (1972) J. Chem. Soc., Chem. Commun. , pp. 466-467
    • Kinugasa, M.1    Hashimoto, S.2
  • 109
    • 3042527462 scopus 로고    scopus 로고
    • β-Lactam Synthesis by the Kinugasa Reaction
    • Marco-Contelles, J. β-Lactam Synthesis by the Kinugasa Reaction Angew. Chem., Int. Ed. 2004, 43, 2198 - 2200
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 2198-2200
    • Marco-Contelles, J.1
  • 110
    • 84907477467 scopus 로고    scopus 로고
    • Kinugasa Reaction: An ‘Ugly Duckling' of β-Lactam Chemistry
    • Stecko, S.; Furman, B.; Chmielewski, M. Kinugasa Reaction: An ‘Ugly Duckling' of β-Lactam Chemistry Tetrahedron 2014, 70, 7817 - 7844
    • (2014) Tetrahedron , vol.70 , pp. 7817-7844
    • Stecko, S.1    Furman, B.2    Chmielewski, M.3
  • 111
    • 37049108147 scopus 로고
    • Cis- and Trans-Azetidin-2-ones from Nitrones and Copper Acetylide
    • Ding, L. K.; Irwin, W. J. Cis- and Trans-Azetidin-2-ones from Nitrones and Copper Acetylide J. Chem. Soc., Perkin Trans. 1 1976, 2382 - 2386
    • (1976) J. Chem. Soc., Perkin Trans. 1 , pp. 2382-2386
    • Ding, L.K.1    Irwin, W.J.2
  • 112
    • 37049074608 scopus 로고
    • Copper-Catalysed Reaction of Arylacetylenes with C,N-Diarylnitrones
    • Okuro, K.; Enna, M.; Miura, M.; Nomura, M. Copper-Catalysed Reaction of Arylacetylenes with C,N-Diarylnitrones J. Chem. Soc., Chem. Commun. 1993, 1107 - 1108
    • (1993) J. Chem. Soc., Chem. Commun. , pp. 1107-1108
    • Okuro, K.1    Enna, M.2    Miura, M.3    Nomura, M.4
  • 113
    • 0029089453 scopus 로고
    • Copper-Catalyzed Reaction of Terminal Alkynes with Nitrones. Selective Synthesis of 1-Aza-1-buten-3-yne and 2-Azetidinone Derivatives
    • Miura, M.; Enna, M.; Okuro, K.; Nomura, M. Copper-Catalyzed Reaction of Terminal Alkynes with Nitrones. Selective Synthesis of 1-Aza-1-buten-3-yne and 2-Azetidinone Derivatives J. Org. Chem. 1995, 60, 4999 - 5004
    • (1995) J. Org. Chem. , vol.60 , pp. 4999-5004
    • Miura, M.1    Enna, M.2    Okuro, K.3    Nomura, M.4
  • 114
    • 0036570894 scopus 로고    scopus 로고
    • Cu(I)/Bis(azaferrocene)-Catalyzed Enantioselective Synthesis of β-Lactams via Couplings of Alkynes with Nitrones
    • Lo, M. M.-C.; Fu, G. C. Cu(I)/Bis(azaferrocene)-Catalyzed Enantioselective Synthesis of β-Lactams via Couplings of Alkynes with Nitrones J. Am. Chem. Soc. 2002, 124, 4572 - 4573
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 4572-4573
    • Lo, M.M.-C.1    Fu, G.C.2
  • 115
    • 0141788715 scopus 로고    scopus 로고
    • Catalytic Enantioselective Synthesis of β-Lactams: Intramolecular Kinugasa Reactions and Interception of an Intermediate in the Reaction Cascade
    • Shintani, R.; Fu, G. C. Catalytic Enantioselective Synthesis of β-Lactams: Intramolecular Kinugasa Reactions and Interception of an Intermediate in the Reaction Cascade Angew. Chem., Int. Ed. 2003, 42, 4082 - 4085
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 4082-4085
    • Shintani, R.1    Fu, G.C.2
  • 116
    • 0142094051 scopus 로고    scopus 로고
    • Chiral Tris(oxazoline)/Cu(II) Catalyzed Coupling of Terminal Alkynes and Nitrones
    • Ye, M.-C.; Zhou, J.; Huang, Z.-Z.; Tang, Y. Chiral Tris(oxazoline)/Cu(II) Catalyzed Coupling of Terminal Alkynes and Nitrones Chem. Commun. 2003, 2554 - 2555
    • (2003) Chem. Commun. , pp. 2554-2555
    • Ye, M.-C.1    Zhou, J.2    Huang, Z.-Z.3    Tang, Y.4
  • 117
    • 33646245219 scopus 로고    scopus 로고
    • Trisoxazoline/Cu(II)-Promoted Kinugasa Reaction. Enantioselective Synthesis of β-Lactams
    • Ye, M.-C.; Zhou, J.; Tang, Y. Trisoxazoline/Cu(II)-Promoted Kinugasa Reaction. Enantioselective Synthesis of β-Lactams J. Org. Chem. 2006, 71, 3576 - 3582
    • (2006) J. Org. Chem. , vol.71 , pp. 3576-3582
    • Ye, M.-C.1    Zhou, J.2    Tang, Y.3
  • 118
    • 84861532056 scopus 로고    scopus 로고
    • Tris(oxazoline)/Copper-Catalyzed Coupling of Alkynes qith Nitrones: A Highly Enantioselective Access to β-Lactams
    • Chen, J. H.; Liao, S. H.; Sun, X. L.; Shen, Q.; Tang, Y. Tris(oxazoline)/Copper-Catalyzed Coupling of Alkynes qith Nitrones: A Highly Enantioselective Access to β-Lactams Tetrahedron 2012, 68, 5042 - 5045
    • (2012) Tetrahedron , vol.68 , pp. 5042-5045
    • Chen, J.H.1    Liao, S.H.2    Sun, X.L.3    Shen, Q.4    Tang, Y.5
  • 119
    • 33847147978 scopus 로고    scopus 로고
    • The Asymmetric Synthesis of β-Lactams: HETPHOX/Cu(I) Mediated Synthesis via the Kinugasa Reaction
    • Coyne, A. G.; Müller-Bunz, H.; Guiry, P. J. The Asymmetric Synthesis of β-Lactams: HETPHOX/Cu(I) Mediated Synthesis via the Kinugasa Reaction Tetrahedron: Asymmetry 2007, 18, 199 - 207
    • (2007) Tetrahedron: Asymmetry , vol.18 , pp. 199-207
    • Coyne, A.G.1    Müller-Bunz, H.2    Guiry, P.J.3
  • 120
    • 67650034191 scopus 로고    scopus 로고
    • Enantioselective Synthesis of β-Lactams via the Indabox-Cu(II)-Catalyzed Kinugasa Reaction
    • Saito, T.; Kikuchi, T.; Tanabe, H.; Yahiro, J.; Otani, T. Enantioselective Synthesis of β-Lactams via the Indabox-Cu(II)-Catalyzed Kinugasa Reaction Tetrahedron Lett. 2009, 50, 4969 - 4972
    • (2009) Tetrahedron Lett. , vol.50 , pp. 4969-4972
    • Saito, T.1    Kikuchi, T.2    Tanabe, H.3    Yahiro, J.4    Otani, T.5
  • 121
    • 84878250682 scopus 로고    scopus 로고
    • Asymmetric Synthesis of trans-β-Lactams by a Kinugasa Reaction on Water
    • Chen, Z.; Lin, L.; Wang, M.; Liu, X.; Feng, X. Asymmetric Synthesis of trans-β-Lactams by a Kinugasa Reaction on Water Chem.-Eur. J. 2013, 19, 7561 - 7567
    • (2013) Chem. - Eur. J. , vol.19 , pp. 7561-7567
    • Chen, Z.1    Lin, L.2    Wang, M.3    Liu, X.4    Feng, X.5
  • 122
    • 84981794159 scopus 로고
    • Syntheses by Means of 1-Alkylidene- and 1-(Arylalkylidene)-3-pyrazolidone N,N-Betaines, a New Type of Stable Azomethine Imine
    • Dorn, H.; Otto, A. Syntheses by Means of 1-Alkylidene- and 1-(Arylalkylidene)-3-pyrazolidone N,N-Betaines, a New Type of Stable Azomethine Imine Angew. Chem., Int. Ed. Engl. 1968, 7, 214 - 215
    • (1968) Angew. Chem., Int. Ed. Engl. , vol.7 , pp. 214-215
    • Dorn, H.1    Otto, A.2
  • 123
    • 84981836036 scopus 로고
    • Über die Reaktion von Pyrazolidon-(3) mit Carbonylverbindungen
    • Dorn, H.; Otto, A. Über die Reaktion von Pyrazolidon-(3) mit Carbonylverbindungen Chem. Ber. 1968, 101, 3287 - 3301
    • (1968) Chem. Ber. , vol.101 , pp. 3287-3301
    • Dorn, H.1    Otto, A.2
  • 124
    • 0015841356 scopus 로고
    • The Synthesis and Properties of N-Acylimino-3,4-dihydroisoquinolinium Betaines
    • Tamura, Y.; Minamikawa, J.-i.; Miki, Y.; Okamoto, Y.; Ikeda, M. The Synthesis and Properties of N-Acylimino-3,4-dihydroisoquinolinium Betaines Yakugaku Zasshi 1973, 93, 648 - 653
    • (1973) Yakugaku Zasshi , vol.93 , pp. 648-653
    • Tamura, Y.1    Minamikawa, J.-I.2    Miki, Y.3    Okamoto, Y.4    Ikeda, M.5
  • 125
    • 84876582439 scopus 로고    scopus 로고
    • Synthesis and Reactivity of Unsymmetrical Azomethine Imines Formed Using Alkene Aminocarbonylation
    • Gan, W.; Moon, P. J.; Clavette, C.; Das Neves, N.; Markiewicz, T.; Toderian, A. B.; Beauchemin, A. M. Synthesis and Reactivity of Unsymmetrical Azomethine Imines Formed Using Alkene Aminocarbonylation Org. Lett. 2013, 15, 1890 - 1893
    • (2013) Org. Lett. , vol.15 , pp. 1890-1893
    • Gan, W.1    Moon, P.J.2    Clavette, C.3    Das Neves, N.4    Markiewicz, T.5    Toderian, A.B.6    Beauchemin, A.M.7
  • 126
    • 84883830001 scopus 로고    scopus 로고
    • Synthesis of Azomethine Imines Using an Intramolecular Alkyne Hydrohydrazination Approach
    • Hunt, A. D.; Dion, I.; Das Neves, N.; Taing, S.; Beauchemin, A. M. Synthesis of Azomethine Imines Using an Intramolecular Alkyne Hydrohydrazination Approach J. Org. Chem. 2013, 78, 8847 - 8852
    • (2013) J. Org. Chem. , vol.78 , pp. 8847-8852
    • Hunt, A.D.1    Dion, I.2    Das Neves, N.3    Taing, S.4    Beauchemin, A.M.5
  • 127
    • 84980167410 scopus 로고
    • Intramolecular [4 + 2] and [3 + 2] Cycloadditions in Organic Synthesis
    • Oppolzer, W. Intramolecular [4 + 2] and [3 + 2] Cycloadditions in Organic Synthesis Angew. Chem., Int. Ed. Engl. 1977, 16, 10 - 23
    • (1977) Angew. Chem., Int. Ed. Engl. , vol.16 , pp. 10-23
    • Oppolzer, W.1
  • 128
    • 0042234004 scopus 로고    scopus 로고
    • A New Copper-Catalyzed [3 + 2] Cycloaddition: Enantioselective Coupling of Terminal Alkynes with Azomethine Imines to Generate Five-Membered Nitrogen Heterocycles
    • Shintani, R.; Fu, G. C. A New Copper-Catalyzed [3 + 2] Cycloaddition: Enantioselective Coupling of Terminal Alkynes with Azomethine Imines To Generate Five-Membered Nitrogen Heterocycles J. Am. Chem. Soc. 2003, 125, 10778 - 10779
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 10778-10779
    • Shintani, R.1    Fu, G.C.2
  • 129
    • 84861503212 scopus 로고    scopus 로고
    • Chiral Bis(imidazolidine)pyridine-Cu Complex-Catalyzed Enantioselective [3 + 2]-Cycloaddition of Azomethine Imines with Propiolates
    • Arai, T.; Ogino, Y. Chiral Bis(imidazolidine)pyridine-Cu Complex-Catalyzed Enantioselective [3 + 2]-Cycloaddition of Azomethine Imines with Propiolates Molecules 2012, 17, 6170 - 6178
    • (2012) Molecules , vol.17 , pp. 6170-6178
    • Arai, T.1    Ogino, Y.2
  • 130
    • 84881413807 scopus 로고    scopus 로고
    • Development of a Tailor-Made Bis(oxazolidine)pyridine-Metal Catalyst for the [3 + 2] Cycloaddition of Azomethine Imines with Propiolates
    • Arai, T.; Ogino, Y.; Sato, T. Development of a Tailor-Made Bis(oxazolidine)pyridine-Metal Catalyst for the [3 + 2] Cycloaddition of Azomethine Imines with Propiolates Chem. Commun. 2013, 49, 7776 - 7778
    • (2013) Chem. Commun. , vol.49 , pp. 7776-7778
    • Arai, T.1    Ogino, Y.2    Sato, T.3
  • 131
    • 23844457533 scopus 로고    scopus 로고
    • Kinetic Resolutions of Azomethine Imines via Copper-Catalyzed [3 + 2] Cycloadditions
    • Suárez, A.; Downey, C. W.; Fu, G. C. Kinetic Resolutions of Azomethine Imines via Copper-Catalyzed [3 + 2] Cycloadditions J. Am. Chem. Soc. 2005, 127, 11244 - 11245
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 11244-11245
    • Suárez, A.1    Downey, C.W.2    Fu, G.C.3
  • 132
    • 80052605589 scopus 로고    scopus 로고
    • Catalytic Asymmetric Alkynylation of C1-Substituted C,N-Cyclic Azomethine Imines by CuI/Chiral Bronsted Acid Co-Catalyst
    • Hashimoto, T.; Omote, M.; Maruoka, K. Catalytic Asymmetric Alkynylation of C1-Substituted C,N-Cyclic Azomethine Imines by CuI/Chiral Bronsted Acid Co-Catalyst Angew. Chem., Int. Ed. 2011, 50, 8952 - 8955
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 8952-8955
    • Hashimoto, T.1    Omote, M.2    Maruoka, K.3
  • 133
    • 84870876853 scopus 로고    scopus 로고
    • Group 11 Metal Amide-Catalyzed Asymmetric Cycloaddition Reactions of Azomethine Imines with Terminal Alkynes
    • Imaizumi, T.; Yamashita, Y.; Kobayashi, S. Group 11 Metal Amide-Catalyzed Asymmetric Cycloaddition Reactions of Azomethine Imines with Terminal Alkynes J. Am. Chem. Soc. 2012, 134, 20049 - 20052
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 20049-20052
    • Imaizumi, T.1    Yamashita, Y.2    Kobayashi, S.3
  • 134
    • 84881242550 scopus 로고    scopus 로고
    • Catalytic Asymmetric Three-Component 1,3-Dipolar Cycloaddition of Aldehydes, Hydrazides, and Alkynes
    • Hashimoto, T.; Takiguchi, Y.; Maruoka, K. Catalytic Asymmetric Three-Component 1,3-Dipolar Cycloaddition of Aldehydes, Hydrazides, and Alkynes J. Am. Chem. Soc. 2013, 135, 11473 - 11476
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 11473-11476
    • Hashimoto, T.1    Takiguchi, Y.2    Maruoka, K.3
  • 135
    • 79960692567 scopus 로고    scopus 로고
    • Generation and Exploitation of Acyclic Azomethine Imines in Chiral Bronsted Acid Catalysis
    • Hashimoto, T.; Kimura, H.; Kawamata, Y.; Maruoka, K. Generation and Exploitation of Acyclic Azomethine Imines in Chiral Bronsted Acid Catalysis Nat. Chem. 2011, 3, 642 - 646
    • (2011) Nat. Chem. , vol.3 , pp. 642-646
    • Hashimoto, T.1    Kimura, H.2    Kawamata, Y.3    Maruoka, K.4
  • 136
    • 84863826915 scopus 로고    scopus 로고
    • A Catalytic Asymmetric Ugi-type Reaction with Acyclic Azomethine Imines
    • Hashimoto, T.; Kimura, H.; Kawamata, Y.; Maruoka, K. A Catalytic Asymmetric Ugi-type Reaction With Acyclic Azomethine Imines Angew. Chem., Int. Ed. 2012, 51, 7279 - 7281
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 7279-7281
    • Hashimoto, T.1    Kimura, H.2    Kawamata, Y.3    Maruoka, K.4
  • 137
    • 33846436800 scopus 로고    scopus 로고
    • Highly Enantioselective and Diastereoselective 1,3-Dipolar Cycloaddition Reactions between Azomethine Imines and 3-Acryloyl-2-oxazolidinone Catalyzed by Binaphthyldiimine-Ni(II) Complexes
    • Suga, H.; Funyu, A.; Kakehi, A. Highly Enantioselective and Diastereoselective 1,3-Dipolar Cycloaddition Reactions between Azomethine Imines and 3-Acryloyl-2-oxazolidinone Catalyzed by Binaphthyldiimine-Ni(II) Complexes Org. Lett. 2007, 9, 97 - 100
    • (2007) Org. Lett. , vol.9 , pp. 97-100
    • Suga, H.1    Funyu, A.2    Kakehi, A.3
  • 138
    • 57649136151 scopus 로고    scopus 로고
    • Copper(II)-Catalyzed Exo and Enantioselective Cycloadditions of Azomethine Imines
    • Sibi, M.; Rane, D.; Stanley, L. M.; Soeta, T. Copper(II)-Catalyzed Exo and Enantioselective Cycloadditions of Azomethine Imines Org. Lett. 2008, 10, 2971 - 2974
    • (2008) Org. Lett. , vol.10 , pp. 2971-2974
    • Sibi, M.1    Rane, D.2    Stanley, L.M.3    Soeta, T.4
  • 139
    • 84877848702 scopus 로고    scopus 로고
    • Nickel(II)-Catalyzed Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines with Alkylidene Malonates
    • Li, J.; Lian, X.; Liu, X.; Lin, L.; Feng, X. Nickel(II)-Catalyzed Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines with Alkylidene Malonates Chem.-Eur. J. 2013, 19, 5134 - 5140
    • (2013) Chem. - Eur. J. , vol.19 , pp. 5134-5140
    • Li, J.1    Lian, X.2    Liu, X.3    Lin, L.4    Feng, X.5
  • 140
    • 77950212800 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloaddition of C,N-Cyclic Azomethine Imines with α,β-Unsaturated Aldehydes
    • Hashimoto, T.; Maeda, Y.; Omote, M.; Nakatsu, H.; Maruoka, K. Catalytic Enantioselective 1,3-Dipolar Cycloaddition of C,N-Cyclic Azomethine Imines with α,β-Unsaturated Aldehydes J. Am. Chem. Soc. 2010, 132, 4076 - 4077
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 4076-4077
    • Hashimoto, T.1    Maeda, Y.2    Omote, M.3    Nakatsu, H.4    Maruoka, K.5
  • 141
    • 84885116524 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition of C,N-Cyclic Azomethine Imines to Unsaturated Nitriles Catalyzed by Ni(II)-Pigiphos
    • Milosevic, S.; Togni, A. Enantioselective 1,3-Dipolar Cycloaddition of C,N-Cyclic Azomethine Imines to Unsaturated Nitriles Catalyzed by Ni(II)-Pigiphos J. Org. Chem. 2013, 78, 9638 - 9646
    • (2013) J. Org. Chem. , vol.78 , pp. 9638-9646
    • Milosevic, S.1    Togni, A.2
  • 142
    • 84924692313 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines with Propioloylpyrazoles Induced by Chiral π-Cation Catalysts
    • Hori, M.; Sakakura, A.; Ishihara, K. Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines with Propioloylpyrazoles Induced by Chiral π-Cation Catalysts J. Am. Chem. Soc. 2014, 136, 13198 - 13201
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 13198-13201
    • Hori, M.1    Sakakura, A.2    Ishihara, K.3
  • 143
    • 42049087072 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition Reaction of Azomethine Imines to Allyl Alcohol
    • Kato, T.; Fujinami, S.; Ukaji, Y.; Inomata, K. Asymmetric 1,3-Dipolar Cycloaddition Reaction of Azomethine Imines to Allyl Alcohol Chem. Lett. 2008, 37, 342 - 343
    • (2008) Chem. Lett. , vol.37 , pp. 342-343
    • Kato, T.1    Fujinami, S.2    Ukaji, Y.3    Inomata, K.4
  • 144
    • 77953665800 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Imines to Allyl Alcohol Utilizing Tartaric Acid Ester as a Chiral Auxiliary
    • Tanaka, K.; Kato, T.; Ukaji, Y.; Inomata, K. Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Imines to Allyl Alcohol Utilizing Tartaric Acid Ester as a Chiral Auxiliary Heterocycles 2010, 80, 887 - 893
    • (2010) Heterocycles , vol.80 , pp. 887-893
    • Tanaka, K.1    Kato, T.2    Ukaji, Y.3    Inomata, K.4
  • 145
    • 77956802896 scopus 로고    scopus 로고
    • Asymmetrie 1,3-Dipolar Cycloaddition of Azomethine Imines to Homoallylic Alcohols
    • Tanaka, K.; Kato, T.; Fujinami, S.; Ukaji, Y.; Inomata, K. Asymmetrie 1,3-Dipolar Cycloaddition of Azomethine Imines to Homoallylic Alcohols Chem. Lett. 2010, 39, 1036 - 1038
    • (2010) Chem. Lett. , vol.39 , pp. 1036-1038
    • Tanaka, K.1    Kato, T.2    Fujinami, S.3    Ukaji, Y.4    Inomata, K.5
  • 146
    • 84895061023 scopus 로고    scopus 로고
    • Desymmetrization of 1,4-Pentadien-3-ol by the Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Imines
    • Yoshida, M.; Sassa, N.; Kato, T.; Fujinami, S.; Soeta, T.; Inomata, K.; Ukaji, Y. Desymmetrization of 1,4-Pentadien-3-ol by the Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Imines Chem.-Eur. J. 2014, 20, 2058 - 2064
    • (2014) Chem. - Eur. J. , vol.20 , pp. 2058-2064
    • Yoshida, M.1    Sassa, N.2    Kato, T.3    Fujinami, S.4    Soeta, T.5    Inomata, K.6    Ukaji, Y.7
  • 147
    • 33749348910 scopus 로고    scopus 로고
    • Organocatalytic and Stereoselective [3 + 2] Cycloadditions of Azomethine Imines with α,β-Unsaturated Aldehydes
    • Chen, W.; Yuan, X.-H.; Li, R.; Du, W.; Wu, Y.; Ding, L.-S.; Chen, Y.-C. Organocatalytic And Stereoselective [3 + 2] Cycloadditions of Azomethine Imines with α,β-Unsaturated Aldehydes Adv. Synth. Catal. 2006, 348, 1818 - 1822
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 1818-1822
    • Chen, W.1    Yuan, X.-H.2    Li, R.3    Du, W.4    Wu, Y.5    Ding, L.-S.6    Chen, Y.-C.7
  • 148
    • 77956806905 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition Reactions of Azomethine Imines with Acrolein Catalyzed by L-Proline and Its Derivatives
    • Suga, H.; Arikawa, T.; Itoh, K.; Okumura, Y.; Kakehi, A.; Shiro, M. Asymmetric 1,3-Dipolar Cycloaddition Reactions of Azomethine Imines with Acrolein Catalyzed by L-Proline And Its Derivatives Heterocycles 2010, 81, 1669 - 16868
    • (2010) Heterocycles , vol.81 , pp. 1669-16868
    • Suga, H.1    Arikawa, T.2    Itoh, K.3    Okumura, Y.4    Kakehi, A.5    Shiro, M.6
  • 149
    • 35048856888 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition of Cyclic Enones Catalyzed by Multifunctional Primary Amines: Beneficial Effects of Hydrogen Bonding
    • Chen, W.; Du, W.; Duan, Y.-Z.; Wu, Y.; Yang, S.-Y.; Chen, Y.-C. Enantioselective 1,3-Dipolar Cycloaddition of Cyclic Enones Catalyzed by Multifunctional Primary Amines: Beneficial Effects of Hydrogen Bonding Angew. Chem., Int. Ed. 2007, 46, 7667 - 7670
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 7667-7670
    • Chen, W.1    Du, W.2    Duan, Y.-Z.3    Wu, Y.4    Yang, S.-Y.5    Chen, Y.-C.6
  • 150
    • 84898618037 scopus 로고    scopus 로고
    • Amine-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions of Aldehydes to C,N-Cyclic Azomethine Imines
    • Li, W.; Jia, Q.; Du, Z.; Zhang, K.; Wang, J. Amine-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions of Aldehydes to C,N-Cyclic Azomethine Imines Chem.-Eur. J. 2014, 20, 4559 - 4562
    • (2014) Chem. - Eur. J. , vol.20 , pp. 4559-4562
    • Li, W.1    Jia, Q.2    Du, Z.3    Zhang, K.4    Wang, J.5
  • 151
    • 84901282759 scopus 로고    scopus 로고
    • Asymmetric Synthesis of Tetrahydroquinolines through a [3 + 2] Cycloaddition Controlled by Dienamine Catalysis
    • Li, W.; Wei, J.; Jia, Q.; Du, Z.; Zhang, K.; Wang, J. Asymmetric Synthesis of Tetrahydroquinolines through a [3 + 2] Cycloaddition Controlled by Dienamine Catalysis Chem.-Eur. J. 2014, 20, 6592 - 6596
    • (2014) Chem. - Eur. J. , vol.20 , pp. 6592-6596
    • Li, W.1    Wei, J.2    Jia, Q.3    Du, Z.4    Zhang, K.5    Wang, J.6
  • 152
    • 84909992819 scopus 로고    scopus 로고
    • Control of the Dual Reactivity (Iminium-Dienamine) of β-Arylmethyl α,β-Unsaturated Aldehydes in Organocatalytic 1,3-Dipolar Cycloadditions with N-Benzoyl C,N-Cyclic Azomethine Imines
    • Izquierdo, C.; Esteban, F.; Parra, A.; Alfaro, R.; Alemán, J.; Fraile, A.; Ruano, J. L. G. Control of the Dual Reactivity (Iminium-Dienamine) of β-Arylmethyl α,β-Unsaturated Aldehydes in Organocatalytic 1,3-Dipolar Cycloadditions with N-Benzoyl C,N-Cyclic Azomethine Imines J. Org. Chem. 2014, 79, 10417 - 10433
    • (2014) J. Org. Chem. , vol.79 , pp. 10417-10433
    • Izquierdo, C.1    Esteban, F.2    Parra, A.3    Alfaro, R.4    Alemán, J.5    Fraile, A.6    Ruano, J.L.G.7
  • 153
    • 79953241662 scopus 로고    scopus 로고
    • Asymmetric Inverse-Electron-Demand 1,3-Dipolar Cycloaddition of C,N-Cyclic Azomethine Imines: An Umpolung Strategy
    • Hashimoto, T.; Omote, M.; Maruoka, K. Asymmetric Inverse-Electron-Demand 1,3-Dipolar Cycloaddition of C,N-Cyclic Azomethine Imines: An Umpolung Strategy Angew. Chem., Int. Ed. 2011, 50, 3489 - 3492
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 3489-3492
    • Hashimoto, T.1    Omote, M.2    Maruoka, K.3
  • 154
    • 84907790147 scopus 로고    scopus 로고
    • Organocatalytic Asymmetric Inverse-Electron-Demand 1,3-Dipolar Cycloaddition of N,N′-Cyclic Azomethine Imines
    • Zhu, R.-Y.; Wang, C.-S.; Zheng, J.; Shi, F.; Tu, S.-J. Organocatalytic Asymmetric Inverse-Electron-Demand 1,3-Dipolar Cycloaddition of N,N′-Cyclic Azomethine Imines J. Org. Chem. 2014, 79, 9305 - 9312
    • (2014) J. Org. Chem. , vol.79 , pp. 9305-9312
    • Zhu, R.-Y.1    Wang, C.-S.2    Zheng, J.3    Shi, F.4    Tu, S.-J.5
  • 155
    • 84879958306 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition of Methyleneindolinones and N,N′-Cyclic Azomethine Imines
    • Hong, L.; Kai, M.; Wu, C.; Sun, W.; Zhu, G.; Li, G.; Yao, X.; Wang, R. Enantioselective 1,3-Dipolar Cycloaddition of Methyleneindolinones And N,N′-Cyclic Azomethine Imines Chem. Commun. 2013, 49, 6713 - 6715
    • (2013) Chem. Commun. , vol.49 , pp. 6713-6715
    • Hong, L.1    Kai, M.2    Wu, C.3    Sun, W.4    Zhu, G.5    Li, G.6    Yao, X.7    Wang, R.8
  • 156
    • 82555168490 scopus 로고    scopus 로고
    • Design of Chiral Bis-phosphoric Acid Catalyst Derived from (R)-3,3′-Di(2-hydroxy-3-arylphenyl)binaphthol: Catalytic Enantioselective Diels-Alder Reaction of α,β-Unsaturated Aldehydes with Amidodienes
    • Momiyama, N.; Konno, T.; Furiya, Y.; Iwamoto, T.; Terada, M. Design of Chiral Bis-phosphoric Acid Catalyst Derived from (R)-3,3′-Di(2-hydroxy-3-arylphenyl)binaphthol: Catalytic Enantioselective Diels-Alder Reaction of α,β-Unsaturated Aldehydes with Amidodienes J. Am. Chem. Soc. 2011, 133, 19294 - 19297
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 19294-19297
    • Momiyama, N.1    Konno, T.2    Furiya, Y.3    Iwamoto, T.4    Terada, M.5
  • 157
    • 84887902776 scopus 로고
    • Synthese von Pyrazolidinen
    • Hesse, K.-D. Synthese von Pyrazolidinen Liebigs Ann. Chem. 1971, 743, 50 - 56
    • (1971) Liebigs Ann. Chem. , vol.743 , pp. 50-56
    • Hesse, K.-D.1
  • 158
    • 0002527884 scopus 로고
    • X=Y-ZH Systems as Potential 1,3-Dipoles
    • Grigg, R.; Kemp, J.; Thompson, N. X=Y-ZH Systems as Potential 1,3-Dipoles Tetrahedron Lett. 1978, 19, 2827 - 2830
    • (1978) Tetrahedron Lett. , vol.19 , pp. 2827-2830
    • Grigg, R.1    Kemp, J.2    Thompson, N.3
  • 159
    • 0038062380 scopus 로고
    • Intramolecular Thermal Cycloaddition Reactions of X=Y-ZH Systems to Non-Activated Olefins
    • Grigg, R.; Jordan, M.; Malone, J. F. Intramolecular Thermal Cycloaddition Reactions of X=Y-ZH Systems to Non-Activated Olefins Tetrahedron Lett. 1979, 20, 3877 - 3878
    • (1979) Tetrahedron Lett. , vol.20 , pp. 3877-3878
    • Grigg, R.1    Jordan, M.2    Malone, J.F.3
  • 160
    • 0001628696 scopus 로고
    • X=Y-ZH Systems as Potential 1,3-Dipoles: Part 131. Prototropic Generation of Azomethine Imines from Hydrazones
    • Grigg, R.; Dowling, M.; Jordan, M. W.; Sridharan, V. X=Y-ZH Systems as Potential 1,3-Dipoles: Part 131. Prototropic Generation of Azomethine Imines from Hydrazones Tetrahedron 1987, 43, 5873 - 5886
    • (1987) Tetrahedron , vol.43 , pp. 5873-5886
    • Grigg, R.1    Dowling, M.2    Jordan, M.W.3    Sridharan, V.4
  • 162
    • 0037146071 scopus 로고    scopus 로고
    • Asymmetric Intramolecular [3 + 2] Cycloaddition Reactions of Acylhydrazones/Olefins Using a Chiral Zirconium Catalyst
    • Kobayashi, S.; Shimizu, H.; Yamashita, Y.; Ishitani, H.; Kobayashi, J. Asymmetric Intramolecular [3 + 2] Cycloaddition Reactions of Acylhydrazones/Olefins Using a Chiral Zirconium Catalyst J. Am. Chem. Soc. 2002, 124, 13678 - 13679
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 13678-13679
    • Kobayashi, S.1    Shimizu, H.2    Yamashita, Y.3    Ishitani, H.4    Kobayashi, J.5
  • 163
    • 4544246197 scopus 로고    scopus 로고
    • Zirconium-Catalyzed Enantioselective [3 + 2] Cycloaddition of Hydrazones to Olefins Leading to Optically Active Pyrazolidine, Pyrazoline, and 1,3-Diamine Derivatives
    • Yamashita, Y.; Kobayashi, S. Zirconium-Catalyzed Enantioselective [3 + 2] Cycloaddition of Hydrazones to Olefins Leading to Optically Active Pyrazolidine, Pyrazoline, and 1,3-Diamine Derivatives J. Am. Chem. Soc. 2004, 126, 11279 - 11282
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 11279-11282
    • Yamashita, Y.1    Kobayashi, S.2
  • 164
    • 22244459251 scopus 로고    scopus 로고
    • A Simple and General Chiral Silicon Lewis Acid for Asymmetric Synthesis: Highly Enantioselective [3 + 2] Acylhydrazone-Enol Ether Cycloadditions
    • Shirakawa, S.; Lombardi, P. J.; Leighton, J. L. A Simple and General Chiral Silicon Lewis Acid for Asymmetric Synthesis: Highly Enantioselective [3 + 2] Acylhydrazone-Enol Ether Cycloadditions J. Am. Chem. Soc. 2005, 127, 9974 - 9975
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 9974-9975
    • Shirakawa, S.1    Lombardi, P.J.2    Leighton, J.L.3
  • 165
    • 33845257337 scopus 로고    scopus 로고
    • A Simple, Efficient, and Highly Enantioselective Synthesis of MS-153 Employing a Chiral Silane Lewis Acid-Promoted Acylhydrazone-Enol Ether [3 + 2] Cycloaddition
    • Tran, K.; Leighton, J. L. A Simple, Efficient, and Highly Enantioselective Synthesis of MS-153 Employing a Chiral Silane Lewis Acid-Promoted Acylhydrazone-Enol Ether [3 + 2] Cycloaddition Adv. Synth. Catal. 2006, 348, 2431 - 2436
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 2431-2436
    • Tran, K.1    Leighton, J.L.2
  • 166
    • 52049111424 scopus 로고    scopus 로고
    • An Efficient Asymmetric Synthesis of Manzacidin C
    • Tran, K.; Lombardi, P. J.; Leighton, J. L. An Efficient Asymmetric Synthesis of Manzacidin C Org. Lett. 2008, 10, 3165 - 3167
    • (2008) Org. Lett. , vol.10 , pp. 3165-3167
    • Tran, K.1    Lombardi, P.J.2    Leighton, J.L.3
  • 167
    • 79958149272 scopus 로고    scopus 로고
    • Towards a Catalytic Asymmetric Version of the [3 + 2] Cycloaddition between Hydrazones and Cyclopentadiene
    • Zamfir, A.; Tsogoeva, S. B. Towards a Catalytic Asymmetric Version of the [3 + 2] Cycloaddition between Hydrazones and Cyclopentadiene Synthesis 2011, 1988 - 1992
    • (2011) Synthesis , pp. 1988-1992
    • Zamfir, A.1    Tsogoeva, S.B.2
  • 168
    • 84869037922 scopus 로고    scopus 로고
    • Combining in situ Generated Chiral Silicon Lewis Acid and Chiral Bronsted Acid Catalysts for [3 + 2] Cycloadditions: Cooperative Catalysis as a Convenient Enantioselective Route to Pyrazolidines
    • Serdyuk, O. V.; Zamfir, A.; Hampel, F.; Tsogoeva, S. B. Combining in situ Generated Chiral Silicon Lewis Acid and Chiral Bronsted Acid Catalysts for [3 + 2] Cycloadditions: Cooperative Catalysis as a Convenient Enantioselective Route to Pyrazolidines Adv. Synth. Catal. 2012, 354, 3115 - 3121
    • (2012) Adv. Synth. Catal. , vol.354 , pp. 3115-3121
    • Serdyuk, O.V.1    Zamfir, A.2    Hampel, F.3    Tsogoeva, S.B.4
  • 169
    • 79958079809 scopus 로고    scopus 로고
    • Silicon Lewis Acid Catalyzed [3 + 2] Cycloaddition Reactions of Hydrazones/Cyclopentadiene: Mild Access to Pyrazolidine Derivatives
    • Zamfir, A.; Schenker, S.; Bauer, W.; Clark, T.; Tsogoeva, S. B. Silicon Lewis Acid Catalyzed [3 + 2] Cycloaddition Reactions of Hydrazones/Cyclopentadiene: Mild Access to Pyrazolidine Derivatives Eur. J. Org. Chem. 2011, 3706 - 3709
    • (2011) Eur. J. Org. Chem. , pp. 3706-3709
    • Zamfir, A.1    Schenker, S.2    Bauer, W.3    Clark, T.4    Tsogoeva, S.B.5
  • 170
    • 84871003006 scopus 로고    scopus 로고
    • Asymmetric Bronsted Acid Catalyzed Cycloadditions-Efficient Enantioselective Synthesis of Pyrazolidines, Pyrazolines, and 1,3-Diamines from N-Acyl Hyrazones and Alkenes
    • Rueping, M.; Maji, M. S.; Küçük, H. B.; Atodiresei, I. Asymmetric Bronsted Acid Catalyzed Cycloadditions-Efficient Enantioselective Synthesis of Pyrazolidines, Pyrazolines, And 1,3-Diamines from N-Acyl Hyrazones and Alkenes Angew. Chem., Int. Ed. 2012, 51, 12864 - 12868
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 12864-12868
    • Rueping, M.1    Maji, M.S.2    Küçük, H.B.3    Atodiresei, I.4
  • 172
    • 84906093290 scopus 로고    scopus 로고
    • Catalytic Asymmetric Synthesis of 4-Nitropyrazolidines: An Access to Optically Active 1,2,3-Triamines
    • Lykke, L.; Carlsen, B. D.; Rambo, R. S.; Jorgensen, K. A. Catalytic Asymmetric Synthesis of 4-Nitropyrazolidines: An Access to Optically Active 1,2,3-Triamines J. Am. Chem. Soc. 2014, 136, 11296 - 11299
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 11296-11299
    • Lykke, L.1    Carlsen, B.D.2    Rambo, R.S.3    Jorgensen, K.A.4
  • 173
    • 41849086318 scopus 로고    scopus 로고
    • Regioselective Synthesis of 1,3,5-Tri- and 1,3,4,5-Tetrasubstituted Pyrazoles from N-Arylhydrazones and Nitroolefins
    • Deng, X.; Mani, N. S. Regioselective Synthesis of 1,3,5-Tri- and 1,3,4,5-Tetrasubstituted Pyrazoles from N-Arylhydrazones and Nitroolefins J. Org. Chem. 2008, 73, 2412 - 2415
    • (2008) J. Org. Chem. , vol.73 , pp. 2412-2415
    • Deng, X.1    Mani, N.S.2
  • 174
    • 84891863184 scopus 로고    scopus 로고
    • Regioselective Synthesis of 4-Nitro- or 4-Chloro-Tetrasubstituted Pyrazoles from Hydrazones and β-Halo-β-nitrostyrenes
    • Deng, X.; Liang, J. T.; Mani, N. S. Regioselective Synthesis of 4-Nitro- or 4-Chloro-Tetrasubstituted Pyrazoles from Hydrazones and β-Halo-β-nitrostyrenes Eur. J. Org. Chem. 2014, 410 - 417
    • (2014) Eur. J. Org. Chem. , pp. 410-417
    • Deng, X.1    Liang, J.T.2    Mani, N.S.3
  • 175
    • 0000394567 scopus 로고
    • Reactions of Phenylhydrazones with Electron-Deficient Alkenes
    • Snider, B. B.; Conn, R. S. E.; Sealfon, S. Reactions of Phenylhydrazones with Electron-Deficient Alkenes J. Org. Chem. 1979, 44, 218 - 221
    • (1979) J. Org. Chem. , vol.44 , pp. 218-221
    • Snider, B.B.1    Conn, R.S.E.2    Sealfon, S.3
  • 176
    • 0038127244 scopus 로고    scopus 로고
    • Azomethine Ylides in Organic Synthesis
    • Nájera, C.; Sansano, J. Azomethine Ylides in Organic Synthesis Curr. Org. Chem. 2003, 7, 1105 - 1150
    • (2003) Curr. Org. Chem. , vol.7 , pp. 1105-1150
    • Nájera, C.1    Sansano, J.2
  • 177
    • 26844568111 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylides and Alkenes: The Direct Strategy to Prepare Enantioenriched Highly Substituted Proline Derivatives
    • Nájera, C.; Sansano, J. M. Catalytic Enantioselective 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylides and Alkenes: The Direct Strategy to Prepare Enantioenriched Highly Substituted Proline Derivatives Angew. Chem., Int. Ed. 2005, 44, 6272 - 6276
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 6272-6276
    • Nájera, C.1    Sansano, J.M.2
  • 178
    • 23044431676 scopus 로고    scopus 로고
    • Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides
    • Coldham, I.; Hufton, R. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides Chem. Rev. 2005, 105, 2765 - 2810
    • (2005) Chem. Rev. , vol.105 , pp. 2765-2810
    • Coldham, I.1    Hufton, R.2
  • 179
    • 20444398142 scopus 로고    scopus 로고
    • Chiral Catalysts in the Stereoselective Synthesis of Pyrrolidine Derivatives via Metallo-Azomethine Ylides
    • Husinec, S.; Savic, V. Chiral Catalysts in the Stereoselective Synthesis of Pyrrolidine Derivatives via Metallo-Azomethine Ylides Tetrahedron: Asymmetry 2005, 16, 2047 - 2061
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 2047-2061
    • Husinec, S.1    Savic, V.2
  • 180
    • 33751433159 scopus 로고    scopus 로고
    • Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3 + 2]-Cycloaddition of Azomethine Ylides
    • Pandey, G.; Banerjee, P.; Gadre, S. R. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3 + 2]-Cycloaddition of Azomethine Ylides Chem. Rev. 2006, 106, 4484 - 4517
    • (2006) Chem. Rev. , vol.106 , pp. 4484-4517
    • Pandey, G.1    Banerjee, P.2    Gadre, S.R.3
  • 181
    • 79959795429 scopus 로고    scopus 로고
    • Novel Dipolarophiles and Dipoles in the Metal-Catalyzed Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides
    • Adrio, J.; Carretero, J. C. Novel Dipolarophiles and Dipoles in the Metal-Catalyzed Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides Chem. Commun. 2011, 47, 6784 - 6794
    • (2011) Chem. Commun. , vol.47 , pp. 6784-6794
    • Adrio, J.1    Carretero, J.C.2
  • 182
    • 84907831062 scopus 로고    scopus 로고
    • Recent Advances in the Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides
    • Adrio, J.; Carretero, J. C. Recent Advances in the Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides Chem. Commun. 2014, 50, 12434 - 12446
    • (2014) Chem. Commun. , vol.50 , pp. 12434-12446
    • Adrio, J.1    Carretero, J.C.2
  • 183
    • 84898873012 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Azomethine Ylides for Biology-Oriented Synthesis
    • Narayan, R.; Potowski, M.; Jia, Z. J.; Antonchick, A. P.; Waldmann, H. Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Azomethine Ylides for Biology-Oriented Synthesis Acc. Chem. Res. 2014, 47, 1296 - 1310
    • (2014) Acc. Chem. Res. , vol.47 , pp. 1296-1310
    • Narayan, R.1    Potowski, M.2    Jia, Z.J.3    Antonchick, A.P.4    Waldmann, H.5
  • 184
    • 80051790841 scopus 로고    scopus 로고
    • Enantioselective Synthesis of Proline Derivatives by 1,3-Dipolar Cycloadditions
    • Nájera, C.; Sansano, J. M. Enantioselective Synthesis of Proline Derivatives by 1,3-Dipolar Cycloadditions Monatsh. Chem. 2011, 142, 659 - 680
    • (2011) Monatsh. Chem. , vol.142 , pp. 659-680
    • Nájera, C.1    Sansano, J.M.2
  • 185
    • 84908462648 scopus 로고    scopus 로고
    • Coinage Metal Complexes as Chiral Catalysts for 1,3-Dipolar Cycloadditions
    • Nájera, C.; Sansano, J. M. Coinage Metal Complexes as Chiral Catalysts for 1,3-Dipolar Cycloadditions J. Organomet. Chem. 2014, 771, 78 - 92
    • (2014) J. Organomet. Chem. , vol.771 , pp. 78-92
    • Nájera, C.1    Sansano, J.M.2
  • 186
    • 0026495944 scopus 로고
    • X=Y-ZH Systems as Potential 1,3-Dipoles. Part 39. Metallo-Azomethine Ylides from Aliphatic Aldimines. Facile Regio- and Stereo-Specific Cycloaddition Reactions
    • Grigg, R.; Montgomery, J.; Somasunderam, A. X=Y-ZH Systems as Potential 1,3-Dipoles. Part 39. Metallo-Azomethine Ylides from Aliphatic Aldimines. Facile Regio- and Stereo-Specific Cycloaddition Reactions Tetrahedron 1992, 48, 10431 - 10442 and references therein.
    • (1992) Tetrahedron , vol.48 , pp. 10431-10442
    • Grigg, R.1    Montgomery, J.2    Somasunderam, A.3
  • 187
    • 0026003250 scopus 로고
    • Chiral Co(II) and Mn(II) Catalysts for the 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides Derived from Arylidene Imines of Glycine
    • Allway, P.; Grigg, R. Chiral Co(II) and Mn(II) Catalysts for the 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides Derived from Arylidene Imines of Glycine Tetrahedron Lett. 1991, 32, 5817 - 5820
    • (1991) Tetrahedron Lett. , vol.32 , pp. 5817-5820
    • Allway, P.1    Grigg, R.2
  • 188
    • 0028824566 scopus 로고
    • Asymmetric Cascade 1,3-Dipolar Cycloaddition Reactions of Imines
    • Grigg, R. Asymmetric Cascade 1,3-Dipolar Cycloaddition Reactions of Imines Tetrahedron: Asymmetry 1995, 6, 2475 - 2486
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 2475-2486
    • Grigg, R.1
  • 189
    • 0037073234 scopus 로고    scopus 로고
    • Highly Enantioselective Ag(I)-Catalyzed [3 + 2] Cycloaddition of Azomethine Ylides
    • Longmire, J. M.; Wang, B.; Zhang, X. Highly Enantioselective Ag(I)-Catalyzed [3 + 2] Cycloaddition of Azomethine Ylides J. Am. Chem. Soc. 2002, 124, 13400 - 13401
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 13400-13401
    • Longmire, J.M.1    Wang, B.2    Zhang, X.3
  • 190
    • 0037112719 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides - A Simple Approach to Optically Active Highly Functionalized Proline Derivatives
    • Gothelf, A. S.; Gothelf, K. V.; Hazell, R. G.; Jorgensen, K. A. Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides-A Simple Approach to Optically Active Highly Functionalized Proline Derivatives Angew. Chem., Int. Ed. 2002, 41, 4236 - 4238
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 4236-4238
    • Gothelf, A.S.1    Gothelf, K.V.2    Hazell, R.G.3    Jorgensen, K.A.4
  • 191
    • 27144481089 scopus 로고    scopus 로고
    • A Convenient Procedure for the Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides and Alkenes
    • Alemparte, C.; Blay, G.; Jorgensen, K. A. A Convenient Procedure for the Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides and Alkenes Org. Lett. 2005, 7, 4569 - 4572
    • (2005) Org. Lett. , vol.7 , pp. 4569-4572
    • Alemparte, C.1    Blay, G.2    Jorgensen, K.A.3
  • 193
    • 0041931082 scopus 로고    scopus 로고
    • Catalytic Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides. Development of a Versatile Stepwise, Three-Component Reaction for Diversity-Oriented Synthesis
    • Chen, C.; Li, X.; Schreiber, S. L. Catalytic Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides. Development of a Versatile Stepwise, Three-Component Reaction for Diversity-Oriented Synthesis J. Am. Chem. Soc. 2003, 125, 10174 - 10175
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 10174-10175
    • Chen, C.1    Li, X.2    Schreiber, S.L.3
  • 195
    • 28444438851 scopus 로고    scopus 로고
    • Highly Enantioselective Copper(I)-Fesulphos-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides
    • Cabrera, S.; Arrayás, R. G.; Carretero, J. C. Highly Enantioselective Copper(I)-Fesulphos-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides J. Am. Chem. Soc. 2005, 127, 16394 - 16395
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 16394-16395
    • Cabrera, S.1    Arrayás, R.G.2    Carretero, J.C.3
  • 196
    • 34249702886 scopus 로고    scopus 로고
    • CuI-Fesulphos Complexes: Efficient Chiral Catalysts for Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides
    • Cabrera, S.; Arrayás, R. G.; Martín-Matute, B.; Cossíno, F. P.; Carretero, J. C. CuI-Fesulphos Complexes: Efficient Chiral Catalysts for Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides Tetrahedron 2007, 63, 6587 - 6602
    • (2007) Tetrahedron , vol.63 , pp. 6587-6602
    • Cabrera, S.1    Arrayás, R.G.2    Martín-Matute, B.3    Cossíno, F.P.4    Carretero, J.C.5
  • 198
    • 61449225673 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with α,β-Unsaturated Ketones
    • Hernández-Toribio, J.; Arrayás, R. G.; MartiÌ€n-Matute, B.; Carretero, J. C. Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides With α,β-Unsaturated Ketones Org. Lett. 2009, 11, 393 - 396
    • (2009) Org. Lett. , vol.11 , pp. 393-396
    • Hernández-Toribio, J.1    Arrayás, R.G.2    Martìn-Matute, B.3    Carretero, J.C.4
  • 199
    • 34249318010 scopus 로고    scopus 로고
    • AgOAc Catalyzed Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides with Chiral Ferrocene Derived P,S Ligands
    • Zeng, W.; Zhou, Y.-G. AgOAc Catalyzed Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides with Chiral Ferrocene Derived P,S Ligands Tetrahedron Lett. 2007, 48, 4619 - 4622
    • (2007) Tetrahedron Lett. , vol.48 , pp. 4619-4622
    • Zeng, W.1    Zhou, Y.-G.2
  • 200
    • 77951165292 scopus 로고    scopus 로고
    • Highly Endo-Selective and Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylide with α-Enones Catalyzed by a Silver(I)/Thioclickferrophos Complex
    • Oura, I.; Shimizu, K.; Ogata, K.; Fukuzawa, S. I. Highly Endo-Selective and Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylide with α-Enones Catalyzed by a Silver(I)/Thioclickferrophos Complex Org. Lett. 2010, 12, 1752 - 1755
    • (2010) Org. Lett. , vol.12 , pp. 1752-1755
    • Oura, I.1    Shimizu, K.2    Ogata, K.3    Fukuzawa, S.I.4
  • 201
    • 78549238509 scopus 로고    scopus 로고
    • Ag/Thioclickferrophos Catalyzed Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Alkenes
    • Shimizu, K.; Ogata, K.; Fukuzawa, S. I. Ag/Thioclickferrophos Catalyzed Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Alkenes Tetrahedron Lett. 2010, 51, 5068 - 5070
    • (2010) Tetrahedron Lett. , vol.51 , pp. 5068-5070
    • Shimizu, K.1    Ogata, K.2    Fukuzawa, S.I.3
  • 202
    • 84893720767 scopus 로고    scopus 로고
    • Bifunctional AgOAc/ThioClickFerrophos Complex-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Aryl- and Alkylidene Malonates
    • Watanabe, S.; Tada, A.; Tokoro, Y.; Fukuzawa, S. I. Bifunctional AgOAc/ThioClickFerrophos Complex-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Aryl- and Alkylidene Malonates Tetrahedron Lett. 2014, 55, 1306 - 1309
    • (2014) Tetrahedron Lett. , vol.55 , pp. 1306-1309
    • Watanabe, S.1    Tada, A.2    Tokoro, Y.3    Fukuzawa, S.I.4
  • 203
    • 84908248680 scopus 로고    scopus 로고
    • Synthesis of 7-Azabicyclo[2.2.1]heptane-1-carboxylate via Silver/Thioclickferrophos-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Dihydropyrrole Ester with N-Substituted Maleimide
    • Tada, A.; Watanabe, S.; Kimura, M.; Tokoro, Y.; Fukuzawa, S.-i. Synthesis of 7-Azabicyclo[2.2.1]heptane-1-carboxylate via Silver/Thioclickferrophos-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Dihydropyrrole Ester with N-Substituted Maleimide Tetrahedron Lett. 2014, 55, 6224 - 6226
    • (2014) Tetrahedron Lett. , vol.55 , pp. 6224-6226
    • Tada, A.1    Watanabe, S.2    Kimura, M.3    Tokoro, Y.4    Fukuzawa, S.-I.5
  • 204
    • 78650360096 scopus 로고    scopus 로고
    • New Chiral Ferrocenyl P,S-Ligands for Highly Diastereo-/Enantioselective Catalytic [3 + 2] Cycloaddition of Azomethine Ylides with Cyclic and Acyclic Enones
    • Zhang, C.; Yu, S. B.; Hu, X. P.; Wang, D. Y.; Zheng, Z. New Chiral Ferrocenyl P,S-Ligands for Highly Diastereo-/Enantioselective Catalytic [3 + 2] Cycloaddition of Azomethine Ylides with Cyclic and Acyclic Enones Org. Lett. 2010, 12, 5542 - 5545
    • (2010) Org. Lett. , vol.12 , pp. 5542-5545
    • Zhang, C.1    Yu, S.B.2    Hu, X.P.3    Wang, D.Y.4    Zheng, Z.5
  • 205
    • 84859381033 scopus 로고    scopus 로고
    • New Chiral Ferrocenyl P,S-Ligands for Highly Diastereo- and Enantioselective Ag(I)-Catalyzed Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides
    • Han, M. L.; Wang, D. Y.; Zeng, P. W.; Zheng, Z.; Hu, X. P. New Chiral Ferrocenyl P,S-Ligands for Highly Diastereo- and Enantioselective Ag(I)-Catalyzed Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides Tetrahedron: Asymmetry 2012, 23, 306 - 312
    • (2012) Tetrahedron: Asymmetry , vol.23 , pp. 306-312
    • Han, M.L.1    Wang, D.Y.2    Zeng, P.W.3    Zheng, Z.4    Hu, X.P.5
  • 206
    • 84859871545 scopus 로고    scopus 로고
    • Programmable Enantioselective One-Pot Synthesis of Molecules with Eight Stereocenters
    • Potowski, M.; Schürmann, M.; Preut, H.; Antonchick, A. P.; Waldmann, H. Programmable Enantioselective One-Pot Synthesis of Molecules with Eight Stereocenters Nat. Chem. Biol. 2012, 8, 428 - 430
    • (2012) Nat. Chem. Biol. , vol.8 , pp. 428-430
    • Potowski, M.1    Schürmann, M.2    Preut, H.3    Antonchick, A.P.4    Waldmann, H.5
  • 207
    • 33846594443 scopus 로고    scopus 로고
    • Hydrogen-Bonding Directed Reversal of Enantioselectivity
    • Zeng, W.; Chen, G.-Y.; Zhou, Y.-G.; Li, Y.-X. Hydrogen-Bonding Directed Reversal of Enantioselectivity J. Am. Chem. Soc. 2007, 129, 750 - 751
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 750-751
    • Zeng, W.1    Chen, G.-Y.2    Zhou, Y.-G.3    Li, Y.-X.4
  • 210
    • 84862743186 scopus 로고    scopus 로고
    • Catalytic Asymmetric Exo'-Selective [3 + 2] Cycloaddition for Constructing Stereochemically Diversified Spiro[pyrrolidin-3,3′-oxindole]s
    • Awata, A.; Arai, T. Catalytic Asymmetric Exo'-Selective [3 + 2] Cycloaddition for Constructing Stereochemically Diversified Spiro[pyrrolidin-3,3′-oxindole]s Chem.-Eur. J. 2012, 18, 8278 - 8282
    • (2012) Chem. - Eur. J. , vol.18 , pp. 8278-8282
    • Awata, A.1    Arai, T.2
  • 211
    • 70349928914 scopus 로고    scopus 로고
    • Reversal of Enantioselectivity between the Copper(I)- and Silvers-Catalyzed 1,3-Dipolar Cycloaddition Reactions Using a Brucine-Derived Amino Alcohol Ligand
    • Kim, H. Y.; Shih, H. J.; Knabe, W. E.; Oh, K. Reversal of Enantioselectivity between the Copper(I)- and Silvers-Catalyzed 1,3-Dipolar Cycloaddition Reactions Using a Brucine-Derived Amino Alcohol Ligand Angew. Chem, Int. Ed. 2009, 48, 7420 - 7423
    • (2009) Angew. Chem, Int. Ed. , vol.48 , pp. 7420-7423
    • Kim, H.Y.1    Shih, H.J.2    Knabe, W.E.3    Oh, K.4
  • 212
    • 51449096219 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides and Alkenes by Using Phosphoramidite-Silver(I) Complexes
    • Nájera, C.; Retamosa, M. d. G.; Sansano, J. M. Catalytic Enantioselective 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides and Alkenes by Using Phosphoramidite-Silver(I) Complexes Angew. Chem., Int. Ed. 2008, 47, 6055 - 6058
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 6055-6058
    • Nájera, C.1    Retamosa, M.D.G.2    Sansano, J.M.3
  • 213
    • 70549094240 scopus 로고    scopus 로고
    • Synthesis of Prolines by Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides and Alkenes Catalyzed by Chiral Phosphoramidite-Silver(I) Complexes
    • Nájera, C.; De Retamosa, M. G.; Martín-Rodríguez, M.; Sansano, J. M.; De Cózar, A.; Cossío, F. P. Synthesis of Prolines by Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides and Alkenes Catalyzed by Chiral Phosphoramidite-Silver(I) Complexes Eur. J. Org. Chem. 2009, 5622 - 5634
    • (2009) Eur. J. Org. Chem. , pp. 5622-5634
    • Nájera, C.1    De Retamosa, M.G.2    Martín-Rodríguez, M.3    Sansano, J.M.4    De Cózar, A.5    Cossío, F.P.6
  • 214
    • 67749129322 scopus 로고    scopus 로고
    • Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides Catalyzed by Copper(L)/TF-Biphamphos Complexes
    • Wang, C. J.; Liang, G.; Xue, Z. Y.; Gao, F. Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides Catalyzed by Copper(L)/TF-Biphamphos Complexes J. Am. Chem. Soc. 2008, 130, 17250 - 17251
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 17250-17251
    • Wang, C.J.1    Liang, G.2    Xue, Z.Y.3    Gao, F.4
  • 215
    • 84862513188 scopus 로고    scopus 로고
    • Stereoselective Construction of Spiro(butyrolactonepyrrolidines) by Highly Efficient Copper(I)/TF-Biphamphos-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition
    • Liu, T. L.; He, Z. L.; Tao, H. Y.; Wang, C. J. Stereoselective Construction of Spiro(butyrolactonepyrrolidines) by Highly Efficient Copper(I)/TF-Biphamphos-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Chem.-Eur. J. 2012, 18, 8042 - 8046
    • (2012) Chem. - Eur. J. , vol.18 , pp. 8042-8046
    • Liu, T.L.1    He, Z.L.2    Tao, H.Y.3    Wang, C.J.4
  • 216
    • 85027916904 scopus 로고    scopus 로고
    • Catalytic Asymmetric Construction of Azabicyclo[2.2.1]heptanes Bearing Two Quaternary Stereogenic Centers via Silver(I)-Catalyzed 1,3-Dipolar Cycloaddition of Cyclic Azomethine Ylides
    • Xue, Z.-Y.; Xiong, Y.; Wang, C.-J. Catalytic Asymmetric Construction of Azabicyclo[2.2.1]heptanes Bearing Two Quaternary Stereogenic Centers via Silver(I)-Catalyzed 1,3-Dipolar Cycloaddition of Cyclic Azomethine Ylides Synlett 2014, 25, 2733 - 2737
    • (2014) Synlett , vol.25 , pp. 2733-2737
    • Xue, Z.-Y.1    Xiong, Y.2    Wang, C.-J.3
  • 217
    • 80053299772 scopus 로고    scopus 로고
    • Asymmetric Construction of Trifluoromethylated Pyrrolidines via Cu(I)-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with 4,4,4-Trifluorocrotonates
    • Li, Q. H.; Tong, M. C.; Li, J.; Tao, H. Y.; Wang, C. J. Asymmetric Construction of Trifluoromethylated Pyrrolidines via Cu(I)-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with 4,4,4-Trifluorocrotonates Chem. Commun. 2011, 47, 11110 - 11112
    • (2011) Chem. Commun. , vol.47 , pp. 11110-11112
    • Li, Q.H.1    Tong, M.C.2    Li, J.3    Tao, H.Y.4    Wang, C.J.5
  • 218
    • 79952274301 scopus 로고    scopus 로고
    • Stereoselective Construction of a 5-Aza-spiro[2,4]heptane Motif via Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides and Ethyl Cyclopropylidene Acetate
    • Liu, T. L.; He, Z. L.; Tao, H. Y.; Cai, Y. P.; Wang, C. J. Stereoselective Construction of a 5-Aza-spiro[2,4]heptane Motif via Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides and Ethyl Cyclopropylidene Acetate Chem. Commun. 2011, 47, 2616 - 2618
    • (2011) Chem. Commun. , vol.47 , pp. 2616-2618
    • Liu, T.L.1    He, Z.L.2    Tao, H.Y.3    Cai, Y.P.4    Wang, C.J.5
  • 219
    • 80051736589 scopus 로고    scopus 로고
    • Highly Efficient Construction of Spirocyclic Chromanone-Pyrrolidines via Cu(I)/TF-Biphamphos-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition
    • Liu, T. L.; He, Z. L.; Wang, C. J. Highly Efficient Construction of Spirocyclic Chromanone-Pyrrolidines via Cu(I)/TF-Biphamphos-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Chem. Commun. 2011, 47, 9600 - 9602
    • (2011) Chem. Commun. , vol.47 , pp. 9600-9602
    • Liu, T.L.1    He, Z.L.2    Wang, C.J.3
  • 220
    • 79952182033 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar Cycloaddition of N-Unprotected 2-Oxoindolin-3-Ylidene Derivatives and Azomethine Ylides for the Construction of Spirooxindole-Pyrrolidines
    • Liu, T. L.; Xue, Z. Y.; Tao, H. Y.; Wang, C. J. Catalytic Asymmetric 1,3-Dipolar Cycloaddition of N-Unprotected 2-Oxoindolin-3-Ylidene Derivatives and Azomethine Ylides for the Construction of Spirooxindole-Pyrrolidines Org. Biomol. Chem. 2011, 9, 1980 - 1986
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 1980-1986
    • Liu, T.L.1    Xue, Z.Y.2    Tao, H.Y.3    Wang, C.J.4
  • 221
    • 84897986463 scopus 로고    scopus 로고
    • Cu(I)/TF-Biphamphos-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Dimethyl Itaconate and 2-Methyleneglutarate
    • Tao, H. Y.; He, Z. L.; Yang, Y.; Wang, C. J. Cu(I)/TF-Biphamphos-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Dimethyl Itaconate and 2-Methyleneglutarate RSC Adv. 2014, 4, 16899 - 16905
    • (2014) RSC Adv. , vol.4 , pp. 16899-16905
    • Tao, H.Y.1    He, Z.L.2    Yang, Y.3    Wang, C.J.4
  • 222
    • 79955138869 scopus 로고    scopus 로고
    • Morita-Baylis-Hillman Adducts as Effective Dipolarophiles in Copper(I)-Catalyzed 1,3-Dipolar Cycloaddition with Azomethine Ylides: Asymmetric Construction of Pyrrolidine Derivatives Containing Quaternary Stereogenic Center
    • Teng, H. L.; Huang, H.; Tao, H. Y.; Wang, C. J. Morita-Baylis-Hillman Adducts as Effective Dipolarophiles in Copper(I)-Catalyzed 1,3-Dipolar Cycloaddition with Azomethine Ylides: Asymmetric Construction of Pyrrolidine Derivatives Containing Quaternary Stereogenic Center Chem. Commun. 2011, 47, 5494 - 5496
    • (2011) Chem. Commun. , vol.47 , pp. 5494-5496
    • Teng, H.L.1    Huang, H.2    Tao, H.Y.3    Wang, C.J.4
  • 223
    • 79955439223 scopus 로고    scopus 로고
    • Asymmetric Construction of 3-Vinylidene-Pyrrolidine Derivatives Containing Allene Moiety via Ag(I)/TF-BiphamPhos-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with Diethyl 2-(3,3-Diphenylpropa-1,2-dienylidene) Malonate
    • Xue, Z. Y.; Fang, X.; Wang, C. J. Asymmetric Construction of 3-Vinylidene-Pyrrolidine Derivatives Containing Allene Moiety via Ag(I)/TF-BiphamPhos-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with Diethyl 2-(3,3-Diphenylpropa-1,2-dienylidene) Malonate Org. Biomol. Chem. 2011, 9, 3622 - 3624
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 3622-3624
    • Xue, Z.Y.1    Fang, X.2    Wang, C.J.3
  • 224
    • 77249162351 scopus 로고    scopus 로고
    • Exo-Selective Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Alkylidene Malonates Catalyzed by AgOAc/TF-BiphamPhos
    • Xue, Z. Y.; Liu, T. L.; Lu, Z.; Huang, H.; Tao, H. Y.; Wang, C. J. Exo-Selective Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Alkylidene Malonates Catalyzed by AgOAc/TF-BiphamPhos Chem. Commun. 2010, 46, 1727 - 1729
    • (2010) Chem. Commun. , vol.46 , pp. 1727-1729
    • Xue, Z.Y.1    Liu, T.L.2    Lu, Z.3    Huang, H.4    Tao, H.Y.5    Wang, C.J.6
  • 225
    • 67449100589 scopus 로고    scopus 로고
    • Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides Catalyzed by AgOAc/TF-BiphamPhos
    • Wang, C. J.; Xue, Z. Y.; Liang, G.; Lu, Z. Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides Catalyzed by AgOAc/TF-BiphamPhos Chem. Commun. 2009, 2905 - 2907
    • (2009) Chem. Commun. , pp. 2905-2907
    • Wang, C.J.1    Xue, Z.Y.2    Liang, G.3    Lu, Z.4
  • 226
    • 84880857802 scopus 로고    scopus 로고
    • Asymmetric Construction of Fluorinated Imidazolidines via Cu(I)-Catalyzed Exo′-Selective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Fluorinated Imines
    • Li, Q. H.; Wei, L.; Chen, X.; Wang, C. J. Asymmetric Construction of Fluorinated Imidazolidines via Cu(I)-Catalyzed Exo′-Selective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Fluorinated Imines Chem. Commun. 2013, 49, 6277 - 6279
    • (2013) Chem. Commun. , vol.49 , pp. 6277-6279
    • Li, Q.H.1    Wei, L.2    Chen, X.3    Wang, C.J.4
  • 227
    • 84961979110 scopus 로고    scopus 로고
    • Cu(I)/TF-BiphamPhos Catalyzed Reactions of Alkylidene Bisphosphates and Alkylidene Malonates with Azomethine Ylides: Michael Addition versus 1,3-Dipolar Cycloaddition
    • Wang, M.; Wang, C. J.; Lin, Z. Cu(I)/TF-BiphamPhos Catalyzed Reactions of Alkylidene Bisphosphates and Alkylidene Malonates with Azomethine Ylides: Michael Addition versus 1,3-Dipolar Cycloaddition Organometallics 2012, 31, 7870 - 7876
    • (2012) Organometallics , vol.31 , pp. 7870-7876
    • Wang, M.1    Wang, C.J.2    Lin, Z.3
  • 228
    • 84869484679 scopus 로고    scopus 로고
    • A Facile Access to Fluorinated Pyrrolidines via Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Methyl α-Fluoroacrylate
    • Yan, D.; Li, Q.; Wang, C. A Facile Access to Fluorinated Pyrrolidines via Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Methyl α-Fluoroacrylate Chin. J. Chem. 2012, 30, 2714 - 2720
    • (2012) Chin. J. Chem. , vol.30 , pp. 2714-2720
    • Yan, D.1    Li, Q.2    Wang, C.3
  • 229
    • 79960440533 scopus 로고    scopus 로고
    • Catalytic Asymmetric Construction of Spirocycles Containing Pyrrolidine Motifs and Spiro Quaternary Stereogenic Centers via 1,3-Dipolar Cycloaddition of Azomethine Ylides with 2-Alkylidene-Cycloketones
    • Liu, T. L.; He, Z. L.; Li, Q. H.; Tao, H. Y.; Wang, C. J. Catalytic Asymmetric Construction of Spirocycles Containing Pyrrolidine Motifs and Spiro Quaternary Stereogenic Centers via 1,3-Dipolar Cycloaddition of Azomethine Ylides with 2-Alkylidene-Cycloketones Adv. Synth. Catal. 2011, 353, 1713 - 1719
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 1713-1719
    • Liu, T.L.1    He, Z.L.2    Li, Q.H.3    Tao, H.Y.4    Wang, C.J.5
  • 230
    • 84877155708 scopus 로고    scopus 로고
    • Silver-Catalyzed Enantioselective Desymmetrization: Facile Access to Spirolactone-Pyrrolidines Containing a Spiro Quaternary Stereogenic Center
    • Liu, K.; Teng, H. L.; Yao, L.; Tao, H. Y.; Wang, C. J. Silver-Catalyzed Enantioselective Desymmetrization: Facile Access to Spirolactone-Pyrrolidines Containing a Spiro Quaternary Stereogenic Center Org. Lett. 2013, 15, 2250 - 2253
    • (2013) Org. Lett. , vol.15 , pp. 2250-2253
    • Liu, K.1    Teng, H.L.2    Yao, L.3    Tao, H.Y.4    Wang, C.J.5
  • 231
    • 84871594173 scopus 로고    scopus 로고
    • A Facile Access to Enantioenriched Isoindolines via One-Pot Sequential Cu(I)-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition/Aromatization
    • He, Z.; Liu, T.; Tao, H.; Wang, C. J. A Facile Access to Enantioenriched Isoindolines via One-Pot Sequential Cu(I)-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition/Aromatization Org. Lett. 2012, 14, 6230 - 6233
    • (2012) Org. Lett. , vol.14 , pp. 6230-6233
    • He, Z.1    Liu, T.2    Tao, H.3    Wang, C.J.4
  • 232
    • 34247863739 scopus 로고    scopus 로고
    • Chiral Calcium Complexes as Bronsted Base Catalysts for Asymmetric Addition of α-Amino Acid Derivatives to α,β-Unsaturated Carbonyl Compounds
    • Saito, S.; Tsubogo, T.; Kobayashi, S. Chiral Calcium Complexes as Bronsted Base Catalysts for Asymmetric Addition of α-Amino Acid Derivatives to α,β-Unsaturated Carbonyl Compounds J. Am. Chem. Soc. 2007, 129, 5364 - 5365
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 5364-5365
    • Saito, S.1    Tsubogo, T.2    Kobayashi, S.3
  • 233
    • 53549124720 scopus 로고    scopus 로고
    • Development of Catalytic Asymmetric 1,4-Addition and [3 + 2] Cycloaddition Reactions Using Chiral Calcium Complexes
    • Tsubogo, T.; Saito, S.; Seki, K.; Yamashita, Y.; Kobayashi, S. Development of Catalytic Asymmetric 1,4-Addition and [3 + 2] Cycloaddition Reactions Using Chiral Calcium Complexes J. Am. Chem. Soc. 2008, 130, 13321 - 13332
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 13321-13332
    • Tsubogo, T.1    Saito, S.2    Seki, K.3    Yamashita, Y.4    Kobayashi, S.5
  • 234
    • 0347916937 scopus 로고    scopus 로고
    • Exo- and Enantioselective Cycloaddition of Azomethine Ylides Generated from N-Alkylidene Glycine Esters Using Chiral Phosphine-Copper Complexes
    • Oderaotoshi, Y.; Cheng, W.; Fujitomi, S.; Kasano, Y.; Minakata, S.; Komatsu, M. Exo- and Enantioselective Cycloaddition of Azomethine Ylides Generated from N-Alkylidene Glycine Esters Using Chiral Phosphine-Copper Complexes Org. Lett. 2003, 5, 5043 - 5046
    • (2003) Org. Lett. , vol.5 , pp. 5043-5046
    • Oderaotoshi, Y.1    Cheng, W.2    Fujitomi, S.3    Kasano, Y.4    Minakata, S.5    Komatsu, M.6
  • 235
    • 84861965132 scopus 로고    scopus 로고
    • Cu(I)/DTBM-BIPHEP-Catalyzed Exo-Selective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Cis-Trifluorocrotonate for Asymmetric Construction of Trifluoromethylated Pyrrolidines
    • Li, Q. H.; Xue, Z. Y.; Tao, H. Y.; Wang, C. J. Cu(I)/DTBM-BIPHEP-Catalyzed Exo-Selective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Cis-Trifluorocrotonate for Asymmetric Construction of Trifluoromethylated Pyrrolidines Tetrahedron Lett. 2012, 53, 3650 - 3653
    • (2012) Tetrahedron Lett. , vol.53 , pp. 3650-3653
    • Li, Q.H.1    Xue, Z.Y.2    Tao, H.Y.3    Wang, C.J.4
  • 236
    • 84884609667 scopus 로고    scopus 로고
    • Exo-Selective Construction of Spiro-[butyrolactone-pyrrolidine] via 1,3-Dipolar Cycloaddition of Azomethine Ylides with α-Methylene-γ-butyrolactone Catalyzed by Cu(I)/DTBM-BIPHEP
    • Li, Q.-H.; Liu, T.-L.; Wei, L.; Zhou, X.; Tao, H.-Y.; Wang, C.-J. Exo-Selective Construction of Spiro-[butyrolactone-pyrrolidine] via 1,3-Dipolar Cycloaddition of Azomethine Ylides with α-Methylene-γ-butyrolactone Catalyzed by Cu(I)/DTBM-BIPHEP Chem. Commun. 2013, 49, 9642 - 9644
    • (2013) Chem. Commun. , vol.49 , pp. 9642-9644
    • Li, Q.-H.1    Liu, T.-L.2    Wei, L.3    Zhou, X.4    Tao, H.-Y.5    Wang, C.-J.6
  • 237
    • 25444439300 scopus 로고    scopus 로고
    • Cu(I)-Catalyzed Highly Exo-Selective and Enantioselective [3 + 2] Cycloaddition of Azomethine Ylides with Acrylates
    • Gao, W.; Zhang, X.; Raghunath, M. Cu(I)-Catalyzed Highly Exo-Selective and Enantioselective [3 + 2] Cycloaddition of Azomethine Ylides with Acrylates Org. Lett. 2005, 7, 4241 - 4244
    • (2005) Org. Lett. , vol.7 , pp. 4241-4244
    • Gao, W.1    Zhang, X.2    Raghunath, M.3
  • 238
    • 27644585902 scopus 로고    scopus 로고
    • Bifunctional AgOAc-Catalyzed Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides
    • Zeng, W.; Zhou, Y.-G. Bifunctional AgOAc-Catalyzed Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides Org. Lett. 2005, 7, 5055 - 5058
    • (2005) Org. Lett. , vol.7 , pp. 5055-5058
    • Zeng, W.1    Zhou, Y.-G.2
  • 239
    • 79955779627 scopus 로고    scopus 로고
    • Chiral Silver Amide Catalyst for the [3 + 2] Cycloaddition of α-Amino Esters to Olefins
    • Yamashita, Y.; Imaizumi, T.; Kobayashi, S. Chiral Silver Amide Catalyst for the [3 + 2] Cycloaddition of α-Amino Esters to Olefins Angew. Chem., Int. Ed. 2011, 50, 4893 - 4896
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 4893-4896
    • Yamashita, Y.1    Imaizumi, T.2    Kobayashi, S.3
  • 240
    • 80051763249 scopus 로고    scopus 로고
    • Chiral Silver Amides as Effective Catalysts for Enantioselective [3 + 2] Cycloaddition Reactions
    • Yamashita, Y.; Imaizumi, T.; Guo, X. X.; Kobayashi, S. Chiral Silver Amides as Effective Catalysts for Enantioselective [3 + 2] Cycloaddition Reactions Chem.-Asian J. 2011, 6, 2550 - 2559
    • (2011) Chem. - Asian J. , vol.6 , pp. 2550-2559
    • Yamashita, Y.1    Imaizumi, T.2    Guo, X.X.3    Kobayashi, S.4
  • 242
    • 84896914193 scopus 로고    scopus 로고
    • Catalytic Asymmetric Exo-Selective [C+NC+CC] Reaction
    • Joseph, R.; Murray, C.; Garner, P. Catalytic Asymmetric Exo-Selective [C+NC+CC] Reaction Org. Lett. 2014, 16, 1550 - 1553
    • (2014) Org. Lett. , vol.16 , pp. 1550-1553
    • Joseph, R.1    Murray, C.2    Garner, P.3
  • 243
    • 33748589459 scopus 로고    scopus 로고
    • Asymmetric Multicomponent [C+NC+CC] Synthesis of Highly Functionalized Pyrrolidines Catalyzed by Silver(I)
    • Garner, P.; Kaniskan, H. Ü.; Hu, J.; Youngs, W. J.; Panzner, M. Asymmetric Multicomponent [C+NC+CC] Synthesis of Highly Functionalized Pyrrolidines Catalyzed by Silver(I) Org. Lett. 2006, 8, 3647 - 3650
    • (2006) Org. Lett. , vol.8 , pp. 3647-3650
    • Garner, P.1    Kaniskan, H.Ü.2    Hu, J.3    Youngs, W.J.4    Panzner, M.5
  • 244
    • 35048857747 scopus 로고    scopus 로고
    • Recoverable (R)- and (S)-Binap-Ag(I) Complexes for the Enantioselective 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylides
    • Nájera, C.; Retamosa, M. d. G.; Sansano, J. M. Recoverable (R)- and (S)-Binap-Ag(I) Complexes for the Enantioselective 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylides Org. Lett. 2007, 9, 4025 - 4028
    • (2007) Org. Lett. , vol.9 , pp. 4025-4028
    • Nájera, C.1    Retamosa, M.D.G.2    Sansano, J.M.3
  • 245
    • 59549099912 scopus 로고    scopus 로고
    • Enantioselective Synthesis of Polysubstituted Prolines by Binap-Silver-Catalyzed 1,3-Dipolar Cycloadditions
    • Nájera, C.; de Gracia Retamosa, M.; Sansano, J. M.; Cózar, A. d.; Cossío, F. P. Enantioselective Synthesis of Polysubstituted Prolines by Binap-Silver-Catalyzed 1,3-Dipolar Cycloadditions Tetrahedron: Asymmetry 2008, 19, 2913 - 2923
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 2913-2923
    • Nájera, C.1    De Gracia Retamosa, M.2    Sansano, J.M.3    Cózar, A.D.4    Cossío, F.P.5
  • 246
    • 77956697078 scopus 로고    scopus 로고
    • Binap-Gold(I) Trifluoroacetate as a Bifunctional Catalyst for the Synthesis of Chiral Prolines through 1,3-Dipolar Cycloaddition of Azomethine Ylides
    • Martín-Rodríguez, M.; Nájera, C.; Sansano, J. M.; Wu, F. L. Binap-Gold(I) Trifluoroacetate as a Bifunctional Catalyst for the Synthesis of Chiral Prolines through 1,3-Dipolar Cycloaddition of Azomethine Ylides Tetrahedron: Asymmetry 2010, 21, 1184 - 1186
    • (2010) Tetrahedron: Asymmetry , vol.21 , pp. 1184-1186
    • Martín-Rodríguez, M.1    Nájera, C.2    Sansano, J.M.3    Wu, F.L.4
  • 248
    • 79960781694 scopus 로고    scopus 로고
    • Chiral Gold(I) vs Chiral Silver Complexes as Catalysts for the Enantioselective Synthesis of the Second Generation GSK-Hepatitis C Virus Inhibitor
    • Martín-Rodríguez, M.; Nájera, C.; Sansano, J. M.; De Cózar, A.; Cossío, F. P. Chiral Gold(I) vs Chiral Silver Complexes as Catalysts for The Enantioselective Synthesis of the Second Generation GSK-Hepatitis C Virus Inhibitor Beilstein J. Org. Chem. 2011, 7, 988 - 996
    • (2011) Beilstein J. Org. Chem. , vol.7 , pp. 988-996
    • Martín-Rodríguez, M.1    Nájera, C.2    Sansano, J.M.3    De Cózar, A.4    Cossío, F.P.5
  • 249
    • 82955222360 scopus 로고    scopus 로고
    • Binap-Gold(I) versus Binap-Silver Trifluoroacetate Complexes as Catalysts in 1,3-Dipolar Cycloadditions of Azomethine Ylides
    • Martín-Rodríguez, M.; Nájera, C.; Sansano, J. M.; De Cõzar, A.; Cossío, F. P. Binap-Gold(I) versus Binap-Silver Trifluoroacetate Complexes as Catalysts in 1,3-Dipolar Cycloadditions of Azomethine Ylides Chem.-Eur. J. 2011, 17, 14224 - 14233
    • (2011) Chem. - Eur. J. , vol.17 , pp. 14224-14233
    • Martín-Rodríguez, M.1    Nájera, C.2    Sansano, J.M.3    De Cõzar, A.4    Cossío, F.P.5
  • 251
    • 37549066256 scopus 로고    scopus 로고
    • Axially Chiral BINIM and Ni(II)-Catalyzed Highly Enantioselective 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides and N-Arylmaleimides
    • Shi, J.-W.; Zhao, M.-X.; Lei, Z.-Y.; Shi, M. Axially Chiral BINIM and Ni(II)-Catalyzed Highly Enantioselective 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides and N-Arylmaleimides J. Org. Chem. 2008, 73, 305 - 308
    • (2008) J. Org. Chem. , vol.73 , pp. 305-308
    • Shi, J.-W.1    Zhao, M.-X.2    Lei, Z.-Y.3    Shi, M.4
  • 252
    • 84884537122 scopus 로고    scopus 로고
    • Diastereo- and Enantioselective Three-Component Coupling Approach to Highly Substituted Pyrrolidines
    • Chaulagain, M. R.; Felten, A. E.; Gilbert, K.; Aron, Z. D. Diastereo- and Enantioselective Three-Component Coupling Approach to Highly Substituted Pyrrolidines J. Org. Chem. 2013, 78, 9471 - 9476
    • (2013) J. Org. Chem. , vol.78 , pp. 9471-9476
    • Chaulagain, M.R.1    Felten, A.E.2    Gilbert, K.3    Aron, Z.D.4
  • 253
    • 33750366501 scopus 로고    scopus 로고
    • New Zinc(II)-Based Catalyst for Asymmetric Azomethine Ylide Cycloaddition Reactions
    • Dogan, Ö.; Koyuncu, H.; Garner, P.; Bulut, A.; Youngs, W. J.; Panzner, M. New Zinc(II)-Based Catalyst for Asymmetric Azomethine Ylide Cycloaddition Reactions Org. Lett. 2006, 8, 4687 - 4690
    • (2006) Org. Lett. , vol.8 , pp. 4687-4690
    • Dogan, Ö.1    Koyuncu, H.2    Garner, P.3    Bulut, A.4    Youngs, W.J.5    Panzner, M.6
  • 254
    • 78649328279 scopus 로고    scopus 로고
    • A New Chiral Phosphine Oxide Ligand for Enantioselective 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides
    • Eröksüz, S.; Dogan, Ö.; Garner, P. P. A New Chiral Phosphine Oxide Ligand for Enantioselective 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides Tetrahedron: Asymmetry 2010, 21, 2535 - 2541
    • (2010) Tetrahedron: Asymmetry , vol.21 , pp. 2535-2541
    • Eröksüz, S.1    Dogan, Ö.2    Garner, P.P.3
  • 256
    • 78751580446 scopus 로고    scopus 로고
    • A Novel Fe(II)/Diaryl Prolinol Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Alkenes
    • Wu, H.; Wang, B.; Liu, H.; Wang, L. A Novel Fe(II)/Diaryl Prolinol Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with Alkenes Tetrahedron 2011, 67, 1210 - 1215
    • (2011) Tetrahedron , vol.67 , pp. 1210-1215
    • Wu, H.1    Wang, B.2    Liu, H.3    Wang, L.4
  • 257
    • 84878754913 scopus 로고    scopus 로고
    • Synthesis of New Chiral Ferrocenyl P,N-Ligands with a Benzoxazole Ring and their Application in Ag-Catalyzed Asymmetric [3 + 2] Cycloaddition
    • Yan, S.; Zhang, C.; Wang, Y. H.; Cao, Z.; Zheng, Z.; Hu, X. P. Synthesis of New Chiral Ferrocenyl P,N-Ligands with a Benzoxazole Ring and their Application in Ag-Catalyzed Asymmetric [3 + 2] Cycloaddition Tetrahedron Lett. 2013, 54, 3669 - 3672
    • (2013) Tetrahedron Lett. , vol.54 , pp. 3669-3672
    • Yan, S.1    Zhang, C.2    Wang, Y.H.3    Cao, Z.4    Zheng, Z.5    Hu, X.P.6
  • 258
    • 65349180780 scopus 로고    scopus 로고
    • Enantioselective Ag(I)-Catalyzed [3 + 2] Cycloaddition of Azomethine Ylides Using a Chiral Ferrocene-Based Phosphine-Phosphoramidite Ligand Having a Stereogenic P-Center
    • Yu, S. B.; Hu, X. P.; Deng, J.; Wang, D. Y.; Duan, Z. C.; Zheng, Z. Enantioselective Ag(I)-Catalyzed [3 + 2] Cycloaddition of Azomethine Ylides Using a Chiral Ferrocene-Based Phosphine-Phosphoramidite Ligand Having a Stereogenic P-Center Tetrahedron: Asymmetry 2009, 20, 621 - 625
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 621-625
    • Yu, S.B.1    Hu, X.P.2    Deng, J.3    Wang, D.Y.4    Duan, Z.C.5    Zheng, Z.6
  • 259
    • 84867901560 scopus 로고    scopus 로고
    • Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides Catalyzed by Silver(I) Triflate with a Chiral Bipyrrolidine-Derived Phosphine Ligand
    • Gu, X.; Xu, Z.-J.; Lo, V. K.-Y.; Che, C.-M. Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides Catalyzed by Silver(I) Triflate with a Chiral Bipyrrolidine-Derived Phosphine Ligand Synthesis 2012, 44, 3307 - 3314
    • (2012) Synthesis , vol.44 , pp. 3307-3314
    • Gu, X.1    Xu, Z.-J.2    Lo, V.K.-Y.3    Che, C.-M.4
  • 260
    • 79953893777 scopus 로고    scopus 로고
    • Silver-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with β-Boryl Acrylates
    • López-Pérez, A.; Segler, M.; Adrio, J.; Carretero, J. C. Silver-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with β-Boryl Acrylates J. Org. Chem. 2011, 76, 1945 - 1948
    • (2011) J. Org. Chem. , vol.76 , pp. 1945-1948
    • López-Pérez, A.1    Segler, M.2    Adrio, J.3    Carretero, J.C.4
  • 261
    • 84876948656 scopus 로고    scopus 로고
    • Enantioselective Synthesis of 4-Aminopyrrolidine-2,4-Dicarboxylate Derivatives via Ag-Catalyzed Cycloaddition of Azomethine Ylides with Alkylidene Azlactones
    • González-Esguevillas, M.; Adrio, J.; Carretero, J. C. Enantioselective Synthesis of 4-Aminopyrrolidine-2,4-Dicarboxylate Derivatives via Ag-Catalyzed Cycloaddition of Azomethine Ylides with Alkylidene Azlactones Chem. Commun. 2013, 49, 4649 - 4651
    • (2013) Chem. Commun. , vol.49 , pp. 4649-4651
    • González-Esguevillas, M.1    Adrio, J.2    Carretero, J.C.3
  • 262
    • 84877775101 scopus 로고    scopus 로고
    • Catalytic Asymmetric Construction of Quaternary α-Amino Acid Containing Pyrrolidines through 1,3-Dipolar Cycloaddition of Azomethine Ylides to α-Aminoacrylates
    • Wang, Z.; Luo, S.; Zhang, S.; Yang, W. L.; Liu, Y. Z.; Li, H.; Luo, X.; Deng, W. P. Catalytic Asymmetric Construction of Quaternary α-Amino Acid Containing Pyrrolidines through 1,3-Dipolar Cycloaddition of Azomethine Ylides to α-Aminoacrylates Chem.-Eur. J. 2013, 19, 6739 - 6745
    • (2013) Chem. - Eur. J. , vol.19 , pp. 6739-6745
    • Wang, Z.1    Luo, S.2    Zhang, S.3    Yang, W.L.4    Liu, Y.Z.5    Li, H.6    Luo, X.7    Deng, W.P.8
  • 263
    • 84908628167 scopus 로고    scopus 로고
    • A Rapid and Divergent Access to Chiral Azacyclic Nucleoside Analogues via Highly Enantioselective 1,3-Dipolar Cycloaddition of β-Nucleobase Substituted Acrylates
    • Yang, Q.-L.; Xie, M.-S.; Xia, C.; Sun, H.-L.; Zhang, D.-J.; Huang, K.-X.; Guo, Z.; Qu, G.-R.; Guo, H.-M. A Rapid and Divergent Access to Chiral Azacyclic Nucleoside Analogues via Highly Enantioselective 1,3-Dipolar Cycloaddition of β-Nucleobase Substituted Acrylates Chem. Commun. 2014, 50, 14809 - 14812
    • (2014) Chem. Commun. , vol.50 , pp. 14809-14812
    • Yang, Q.-L.1    Xie, M.-S.2    Xia, C.3    Sun, H.-L.4    Zhang, D.-J.5    Huang, K.-X.6    Guo, Z.7    Qu, G.-R.8    Guo, H.-M.9
  • 264
    • 20644453128 scopus 로고    scopus 로고
    • Enantio- and Diastereoselective [3 + 2] Cycloadditions of Azomethine Ylides with Ag(I)-Phosphinooxazoline Catalysts
    • Stohler, R.; Wahl, F.; Pfaltz, A. Enantio- and Diastereoselective [3 + 2] Cycloadditions of Azomethine Ylides with Ag(I)-Phosphinooxazoline Catalysts Synthesis 2005, 1431 - 1436
    • (2005) Synthesis , pp. 1431-1436
    • Stohler, R.1    Wahl, F.2    Pfaltz, A.3
  • 265
    • 84922784373 scopus 로고    scopus 로고
    • Highly Enantioselective Intramolecular 1,3-Dipolar Cycloaddition: A Route to Piperidino-Pyrrolizidines
    • Vidadala, S. R.; Golz, C.; Strohmann, C.; Daniliuc, C.-G.; Waldmann, H. Highly Enantioselective Intramolecular 1,3-Dipolar Cycloaddition: A Route to Piperidino-Pyrrolizidines Angew. Chem., Int. Ed. 2015, 54, 651 - 655
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 651-655
    • Vidadala, S.R.1    Golz, C.2    Strohmann, C.3    Daniliuc, C.-G.4    Waldmann, H.5
  • 266
    • 33646453057 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Vinyl Sulfones
    • Llamas, T.; Arrayás, R. G.; Carretero, J. C. Catalytic Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Vinyl Sulfones Org. Lett. 2006, 8, 1795 - 1798
    • (2006) Org. Lett. , vol.8 , pp. 1795-1798
    • Llamas, T.1    Arrayás, R.G.2    Carretero, J.C.3
  • 267
    • 33947581106 scopus 로고    scopus 로고
    • Copper(I)-Catalyzed Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Vinyl Sulfones
    • Llamas, T.; Arrayás, R. G.; Carretero, J. C. Copper(I)-Catalyzed Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Vinyl Sulfones Synthesis 2007, 950 - 956
    • (2007) Synthesis , pp. 950-956
    • Llamas, T.1    Arrayás, R.G.2    Carretero, J.C.3
  • 268
    • 48749088215 scopus 로고    scopus 로고
    • Highly Enantioselective Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylide Catalyzed by a Copper(I)/ClickFerrophos Complex
    • Fukuzawa, S.-i.; Oki, H. Highly Enantioselective Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylide Catalyzed by a Copper(I)/ClickFerrophos Complex Org. Lett. 2008, 10, 1747 - 1750
    • (2008) Org. Lett. , vol.10 , pp. 1747-1750
    • Fukuzawa, S.-I.1    Oki, H.2
  • 269
    • 73349116182 scopus 로고    scopus 로고
    • Silver Acetate/TF-Biphamphos-Catalyzed Endo-Selective Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Vinyl Phenyl Sulfone
    • Liang, G.; Tong, M. C.; Wang, C. J. Silver Acetate/TF-Biphamphos-Catalyzed Endo-Selective Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Vinyl Phenyl Sulfone Adv. Synth. Catal. 2009, 351, 3101 - 3106
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 3101-3106
    • Liang, G.1    Tong, M.C.2    Wang, C.J.3
  • 270
    • 48749094724 scopus 로고    scopus 로고
    • Bis-Sulfonyl Ethylene as Masked Acetylene Equivalent in Catalytic Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides
    • López-Pérez, A.; Adrio, J.; Carretero, J. C. Bis-Sulfonyl Ethylene as Masked Acetylene Equivalent in Catalytic Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides J. Am. Chem. Soc. 2008, 130, 10084 - 10085
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 10084-10085
    • López-Pérez, A.1    Adrio, J.2    Carretero, J.C.3
  • 271
    • 58249098586 scopus 로고    scopus 로고
    • The Phenylsulfonyl Group as a Temporal Regiochemical Controller in the Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides
    • López-Pérez, A.; Adrio, J.; Carretero, J. C. The Phenylsulfonyl Group as a Temporal Regiochemical Controller in the Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides Angew. Chem., Int. Ed. 2009, 48, 340 - 343
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 340-343
    • López-Pérez, A.1    Adrio, J.2    Carretero, J.C.3
  • 272
    • 73449146642 scopus 로고    scopus 로고
    • Cu-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with β-Phenylsulfonyl Enones. Ligand Controlled Diastereoselectivity Reversal
    • Robles-Machín, R.; González-Esguevillas, M.; Adrio, J.; Carretero, J. C. Cu-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides with β-Phenylsulfonyl Enones. Ligand Controlled Diastereoselectivity Reversal J. Org. Chem. 2010, 75, 233 - 236
    • (2010) J. Org. Chem. , vol.75 , pp. 233-236
    • Robles-Machín, R.1    González-Esguevillas, M.2    Adrio, J.3    Carretero, J.C.4
  • 273
    • 80555127296 scopus 로고    scopus 로고
    • Unusual Ester-Directed Regiochemical Control in Endo-Selective Asymmetric 1,3-Dipolar Cycloadditions of Azomethine Ylides with β-Sulfonyl Acrylates
    • Tong, M. C.; Li, J.; Tao, H. Y.; Li, Y. X.; Wang, C. J. Unusual Ester-Directed Regiochemical Control in Endo-Selective Asymmetric 1,3-Dipolar Cycloadditions of Azomethine Ylides with β-Sulfonyl Acrylates Chem.-Eur. J. 2011, 17, 12922 - 12927
    • (2011) Chem. - Eur. J. , vol.17 , pp. 12922-12927
    • Tong, M.C.1    Li, J.2    Tao, H.Y.3    Li, Y.X.4    Wang, C.J.5
  • 274
    • 0001741213 scopus 로고    scopus 로고
    • Stereocontrolled Synthesis of Highly Substituted Proline Esters via [3 + 2] Cycloaddition between N-Metalated Azomethine Ylides and Nitroalkenes. Origins of the Metal Effect on the Stereochemical Outcome
    • Ayerbe, M.; Arrieta, A.; Cossío, F. P.; Linden, A. Stereocontrolled Synthesis of Highly Substituted Proline Esters via [3 + 2] Cycloaddition between N-Metalated Azomethine Ylides and Nitroalkenes. Origins of the Metal Effect on the Stereochemical Outcome J. Org. Chem. 1998, 63, 1795 - 1805
    • (1998) J. Org. Chem. , vol.63 , pp. 1795-1805
    • Ayerbe, M.1    Arrieta, A.2    Cossío, F.P.3    Linden, A.4
  • 275
    • 0034725364 scopus 로고    scopus 로고
    • Origins of the Loss of Concertedness in Pericyclic Reactions: Theoretical Prediction and Direct Observation of Stepwise Mechanisms in [3 + 2] Thermal Cycloadditions
    • Vivanco, S.; Lecea, B.; Arrieta, A.; Prieto, P.; Morao, I.; Linden, A.; Cossío, F. P. Origins of the Loss of Concertedness in Pericyclic Reactions: Theoretical Prediction and Direct Observation of Stepwise Mechanisms in [3 + 2] Thermal Cycloadditions J. Am. Chem. Soc. 2000, 122, 6078 - 6092
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 6078-6092
    • Vivanco, S.1    Lecea, B.2    Arrieta, A.3    Prieto, P.4    Morao, I.5    Linden, A.6    Cossío, F.P.7
  • 276
    • 33746290157 scopus 로고    scopus 로고
    • A Highly Enantio- and Diastereoselective Cu-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with Nitroalkenes
    • Yan, X.-X.; Peng, Q.; Zhang, Y.; Zhang, K.; Hong, W.; Hou, X.-L.; Wu, Y.-D. A Highly Enantio- and Diastereoselective Cu-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with Nitroalkenes Angew. Chem., Int. Ed. 2006, 45, 1979 - 1983
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 1979-1983
    • Yan, X.-X.1    Peng, Q.2    Zhang, Y.3    Zhang, K.4    Hong, W.5    Hou, X.-L.6    Wu, Y.-D.7
  • 277
    • 84855730820 scopus 로고    scopus 로고
    • Diastereo- and Enantioselective Synthesis of Fluorinated Proline Derivatives via Copper(I)-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition
    • Li, Q.; Ding, C. H.; Li, X. H.; Weissensteiner, W.; Hou, X. L. Diastereo- and Enantioselective Synthesis of Fluorinated Proline Derivatives via Copper(I)-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Synthesis 2012, 265 - 271
    • (2012) Synthesis , pp. 265-271
    • Li, Q.1    Ding, C.H.2    Li, X.H.3    Weissensteiner, W.4    Hou, X.L.5
  • 279
    • 77951055644 scopus 로고    scopus 로고
    • 2: Catalytic Asymmetric Endo-Selective [3 + 2] Cycloaddition of Imino Esters with Nitroalkenes
    • 2: Catalytic Asymmetric Endo-Selective [3 + 2] Cycloaddition of Imino Esters with Nitroalkenes J. Am. Chem. Soc. 2010, 132, 5338 - 5339
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 5338-5339
    • Arai, T.1    Mishiro, A.2    Yokoyama, N.3    Suzuki, K.4    Sato, H.5
  • 280
    • 78349303425 scopus 로고    scopus 로고
    • Catalytic Asymmetric Exo′-Selective [3 + 2] Cycloaddition of Iminoesters with Nitroalkenes
    • Arai, T.; Yokoyama, N.; Mishiro, A.; Sato, H. Catalytic Asymmetric Exo′-Selective [3 + 2] Cycloaddition of Iminoesters with Nitroalkenes Angew. Chem., Int. Ed. 2010, 49, 7895 - 7898
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 7895-7898
    • Arai, T.1    Yokoyama, N.2    Mishiro, A.3    Sato, H.4
  • 281
    • 84555177970 scopus 로고    scopus 로고
    • Stereodivergency in Catalytic Asymmetric Conjugate Addition Reactions of Glycine (Ket)Imines
    • Kim, H. Y.; Li, J. Y.; Kim, S.; Oh, K. Stereodivergency in Catalytic Asymmetric Conjugate Addition Reactions of Glycine (Ket)Imines J. Am. Chem. Soc. 2011, 133, 20750 - 20753
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 20750-20753
    • Kim, H.Y.1    Li, J.Y.2    Kim, S.3    Oh, K.4
  • 282
    • 84888620843 scopus 로고    scopus 로고
    • Catalytic Enantioselective Synthesis of Functionalized Tropanes Reveals Novel Inhibitors of Hedgehog Signaling
    • Narayan, R.; Bauer, J. O.; Strohmann, C.; Antonchick, A. P.; Waldmann, H. Catalytic Enantioselective Synthesis of Functionalized Tropanes Reveals Novel Inhibitors of Hedgehog Signaling Angew. Chem., Int. Ed. 2013, 52, 12892 - 12896
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 12892-12896
    • Narayan, R.1    Bauer, J.O.2    Strohmann, C.3    Antonchick, A.P.4    Waldmann, H.5
  • 283
    • 84908499994 scopus 로고    scopus 로고
    • PyBidine/Copper Catalyst: Asymmetric Exo′-Selective [3 + 2] Cycloaddition using Imino Ester and Electrophilic Indole
    • Awata, A.; Arai, T. PyBidine/Copper Catalyst: Asymmetric Exo′-Selective [3 + 2] Cycloaddition using Imino Ester and Electrophilic Indole Angew. Chem., Int. Ed. 2014, 53, 10462 - 10465
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 10462-10465
    • Awata, A.1    Arai, T.2
  • 284
    • 70349558255 scopus 로고    scopus 로고
    • An Efficient Approach to Chiral Fullerene Derivatives by Catalytic Enantioselective 1,3-Dipolar Cycloadditions
    • Filippone, S.; Maroto, E. E.; Martín-Domenech, A.; Suarez, M.; Martín, N. An Efficient Approach to Chiral Fullerene Derivatives by Catalytic Enantioselective 1,3-Dipolar Cycloadditions Nat. Chem. 2009, 1, 578 - 582
    • (2009) Nat. Chem. , vol.1 , pp. 578-582
    • Filippone, S.1    Maroto, E.E.2    Martín-Domenech, A.3    Suarez, M.4    Martín, N.5
  • 287
    • 0141741220 scopus 로고    scopus 로고
    • Hetero [6 + 3] Cycloaddition of Fulvenes with N-Alkylidene Glycine Esters: A Facile Synthesis of the Delavayine and Incarvillateine Framework
    • Hong, B.-C.; Gupta, A. K.; Wu, M.-F.; Liao, J.-H.; Lee, G.-H. Hetero [6 + 3] Cycloaddition of Fulvenes with N-Alkylidene Glycine Esters: A Facile Synthesis of the Delavayine and Incarvillateine Framework Org. Lett. 2003, 5, 1689 - 1692
    • (2003) Org. Lett. , vol.5 , pp. 1689-1692
    • Hong, B.-C.1    Gupta, A.K.2    Wu, M.-F.3    Liao, J.-H.4    Lee, G.-H.5
  • 289
    • 84881439385 scopus 로고    scopus 로고
    • Catalytic Asymmetric Exo-Selective [6 + 3] Cycloaddition of Iminoesters with Fulvenes
    • Potowski, M.; Antonchick, A. P.; Waldmann, H. Catalytic Asymmetric Exo-Selective [6 + 3] Cycloaddition of Iminoesters with Fulvenes Chem. Commun. 2013, 49, 7800 - 7802
    • (2013) Chem. Commun. , vol.49 , pp. 7800-7802
    • Potowski, M.1    Antonchick, A.P.2    Waldmann, H.3
  • 290
    • 84874591056 scopus 로고    scopus 로고
    • Fulvenes as Effective Dipolarophiles in Copper(I)-Catalyzed [6 + 3] Cycloaddition of Azomethine Ylides: Asymmetric Construction of Piperidine Derivatives
    • He, Z. L.; Teng, H. L.; Wang, C. J. Fulvenes as Effective Dipolarophiles in Copper(I)-Catalyzed [6 + 3] Cycloaddition of Azomethine Ylides: Asymmetric Construction of Piperidine Derivatives Angew. Chem., Int. Ed. 2013, 52, 2934 - 2938
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 2934-2938
    • He, Z.L.1    Teng, H.L.2    Wang, C.J.3
  • 291
    • 84896736944 scopus 로고    scopus 로고
    • A Facile Access to Piperidine Derivatives via Copper(I)-Catalyzed 1,3-Dipolar [6 + 3] Cycloadditions of Azomethine Ylides with Fulvenes
    • Tao, H. Y.; Wang, C. J. A Facile Access to Piperidine Derivatives via Copper(I)-Catalyzed 1,3-Dipolar [6 + 3] Cycloadditions of Azomethine Ylides with Fulvenes Synlett 2014, 25, 461 - 465
    • (2014) Synlett , vol.25 , pp. 461-465
    • Tao, H.Y.1    Wang, C.J.2
  • 292
    • 84896279531 scopus 로고    scopus 로고
    • Cu(I)-Catalyzed Regio- and Stereoselective [6 + 3] Cycloaddition of Azomethine Ylides with Tropone: An Efficient Asymmetric Access to Bridged Azabicyclo[4.3.1]decadienes
    • Teng, H. L.; Yao, L.; Wang, C. J. Cu(I)-Catalyzed Regio- and Stereoselective [6 + 3] Cycloaddition of Azomethine Ylides with Tropone: An Efficient Asymmetric Access to Bridged Azabicyclo[4.3.1]decadienes J. Am. Chem. Soc. 2014, 136, 4075 - 4080
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 4075-4080
    • Teng, H.L.1    Yao, L.2    Wang, C.J.3
  • 293
    • 84902665556 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar [3 + 6] Cycloaddition of Azomethine Ylides with 2-Acyl Cycloheptatrienes: Efficient Construction of Bridged Heterocycles Bearing Piperidine Moiety
    • Li, Q.-H.; Wei, L.; Wang, C. J. Catalytic Asymmetric 1,3-Dipolar [3 + 6] Cycloaddition of Azomethine Ylides with 2-Acyl Cycloheptatrienes: Efficient Construction of Bridged Heterocycles Bearing Piperidine Moiety J. Am. Chem. Soc. 2014, 136, 8685 - 8692
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 8685-8692
    • Li, Q.-H.1    Wei, L.2    Wang, C.J.3
  • 294
    • 84856496716 scopus 로고    scopus 로고
    • Cu-Catalyzed Asymmetric [3 + 2] Cycloaddition of α-Iminoamides with Activated Olefins
    • González-Esguevillas, M.; Adrio, J.; Carretero, J. C. Cu-Catalyzed Asymmetric [3 + 2] Cycloaddition of α-Iminoamides with Activated Olefins Chem. Commun. 2012, 48, 2149 - 2151
    • (2012) Chem. Commun. , vol.48 , pp. 2149-2151
    • González-Esguevillas, M.1    Adrio, J.2    Carretero, J.C.3
  • 295
    • 77951956331 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar Cycloaddition of α-Iminonitriles
    • Robles-Machín, R.; Alonso, I.; Adrio, J.; Carretero, J. C. Catalytic Asymmetric 1,3-Dipolar Cycloaddition of α-Iminonitriles Chem.-Eur. J. 2010, 16, 5286 - 5291
    • (2010) Chem. - Eur. J. , vol.16 , pp. 5286-5291
    • Robles-Machín, R.1    Alonso, I.2    Adrio, J.3    Carretero, J.C.4
  • 296
    • 84896268279 scopus 로고    scopus 로고
    • Silver-Catalyzed Dynamic Systemic Resolution of α-Iminonitriles in a 1,3-Dipolar Cycloaddition Process
    • Hu, L.; Ramström, O. Silver-Catalyzed Dynamic Systemic Resolution of α-Iminonitriles in a 1,3-Dipolar Cycloaddition Process Chem. Commun. 2014, 50, 3792 - 3794
    • (2014) Chem. Commun. , vol.50 , pp. 3792-3794
    • Hu, L.1    Ramström, O.2
  • 297
    • 5644259533 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Highly Substituted Δ1-Pyrrolines: Exo-Selective 1,3-Dipolar Cycloaddition Reactions with Azlactones
    • Peddibhotla, S.; Tepe, J. J. Stereoselective Synthesis of Highly Substituted Δ1-Pyrrolines: Exo-Selective 1,3-Dipolar Cycloaddition Reactions with Azlactones J. Am. Chem. Soc. 2004, 126, 12776 - 12777
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 12776-12777
    • Peddibhotla, S.1    Tepe, J.J.2
  • 298
    • 35548957834 scopus 로고    scopus 로고
    • Au(I)-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions of Münchnones with Electron-Deficient Alkenes
    • Melhado, A. D.; Luparia, M.; Toste, F. D. Au(I)-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions of Münchnones with Electron-Deficient Alkenes J. Am. Chem. Soc. 2007, 129, 12638 - 12639
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 12638-12639
    • Melhado, A.D.1    Luparia, M.2    Toste, F.D.3
  • 299
    • 79952606434 scopus 로고    scopus 로고
    • Gold(I)-Catalyzed Diastereo- and Enantioselective 1,3-Dipolar Cycloaddition and Mannich Reactions of Azlactones
    • Melhado, A. D.; Amarante, G. W.; Wang, Z. J.; Luparia, M.; Toste, F. D. Gold(I)-Catalyzed Diastereo- and Enantioselective 1,3-Dipolar Cycloaddition and Mannich Reactions of Azlactones J. Am. Chem. Soc. 2011, 133, 3517 - 3527
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 3517-3527
    • Melhado, A.D.1    Amarante, G.W.2    Wang, Z.J.3    Luparia, M.4    Toste, F.D.5
  • 300
    • 84655161866 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloadditions of Azlactones and Electrophilic Alkenes Catalyzed by Dimeric BinapAuTFA Complexes
    • Martín-Rodríguez, M.; Nájera, C.; Sansano, J. M. Enantioselective 1,3-Dipolar Cycloadditions of Azlactones and Electrophilic Alkenes Catalyzed by Dimeric BinapAuTFA Complexes Synlett 2012, 62 - 65
    • (2012) Synlett , pp. 62-65
    • Martín-Rodríguez, M.1    Nájera, C.2    Sansano, J.M.3
  • 302
    • 77950462377 scopus 로고    scopus 로고
    • Chiral Silver Amide-Catalyzed Enantioselective [3 + 2] Cycloaddition of α-Aminophosphonates with Olefins
    • Yamashita, Y.; Guo, X.-X.; Takashita, R.; Kobayashi, S. Chiral Silver Amide-Catalyzed Enantioselective [3 + 2] Cycloaddition of α-Aminophosphonates with Olefins J. Am. Chem. Soc. 2010, 132, 3262 - 3263
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 3262-3263
    • Yamashita, Y.1    Guo, X.-X.2    Takashita, R.3    Kobayashi, S.4
  • 303
    • 78650413360 scopus 로고    scopus 로고
    • N-(2-Pyridylmethyl)Imines as Azomethine Precursors in Catalytic Asymmetric [3 + 2] Cycloadditions
    • Padilla, S.; Tejero, R.; Adrio, J.; Carretero, J. C. N-(2-Pyridylmethyl)Imines as Azomethine Precursors in Catalytic Asymmetric [3 + 2] Cycloadditions Org. Lett. 2010, 12, 5608 - 5611
    • (2010) Org. Lett. , vol.12 , pp. 5608-5611
    • Padilla, S.1    Tejero, R.2    Adrio, J.3    Carretero, J.C.4
  • 304
    • 84865411545 scopus 로고    scopus 로고
    • Catalytic Asymmetric Synthesis of α-Quaternary Proline Derivatives by 1,3-Dipolar Cycloaddition of α-Silylimines
    • Hernández-Toribio, J.; Padilla, S.; Adrio, J.; Carretero, J. C. Catalytic Asymmetric Synthesis of α-Quaternary Proline Derivatives by 1,3-Dipolar Cycloaddition of α-Silylimines Angew. Chem., Int. Ed. 2012, 51, 8854 - 8858
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 8854-8858
    • Hernández-Toribio, J.1    Padilla, S.2    Adrio, J.3    Carretero, J.C.4
  • 305
    • 84899015565 scopus 로고    scopus 로고
    • Enantioselective Synthesis of α-Heteroarylpyrrolidines by Copper-Catalyzed 1,3-Dipolar Cycloaddition of α-Silylimines
    • Pascual-Escudero, A.; González-Esguevillas, M.; Padilla, S.; Adrio, J.; Carretero, J. C. Enantioselective Synthesis of α-Heteroarylpyrrolidines by Copper-Catalyzed 1,3-Dipolar Cycloaddition of α-Silylimines Org. Lett. 2014, 16, 2228 - 2231
    • (2014) Org. Lett. , vol.16 , pp. 2228-2231
    • Pascual-Escudero, A.1    González-Esguevillas, M.2    Padilla, S.3    Adrio, J.4    Carretero, J.C.5
  • 306
    • 84894095359 scopus 로고    scopus 로고
    • An Efficient, One-Pot, Three-Component Procedure for the Synthesis of Chiral Spirooxindolopyrrolizidines via Catalytic Highly Enantioselective 1,3-Dipolar Cycloaddition
    • Salahi, F.; Taghizadeh, M. J.; Arvinnezhad, H.; Moemeni, M.; Jadidi, K.; Notash, B. An Efficient, One-Pot, Three-Component Procedure for the Synthesis of Chiral Spirooxindolopyrrolizidines via Catalytic Highly Enantioselective 1,3-Dipolar Cycloaddition Tetrahedron Lett. 2014, 55, 1515 - 1518
    • (2014) Tetrahedron Lett. , vol.55 , pp. 1515-1518
    • Salahi, F.1    Taghizadeh, M.J.2    Arvinnezhad, H.3    Moemeni, M.4    Jadidi, K.5    Notash, B.6
  • 307
    • 34447315556 scopus 로고    scopus 로고
    • Organocatalytic Enantioselective [3 + 2] Cycloaddition of Azomethine Ylides and α,β-Unsaturated Aldehydes
    • Vicario, J. L.; Reboredo, S.; Badía, D.; Carrillo, L. Organocatalytic Enantioselective [3 + 2] Cycloaddition of Azomethine Ylides and α,β-Unsaturated Aldehydes Angew. Chem., Int. Ed. 2007, 46, 5168 - 5170
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 5168-5170
    • Vicario, J.L.1    Reboredo, S.2    Badía, D.3    Carrillo, L.4
  • 308
    • 84861620941 scopus 로고    scopus 로고
    • An Amine-Catalyzed Enantioselective [3 + 2] Cycloaddition of Azomethine Ylides and α,β-Unsaturated Aldehydes: Applications and Mechanistic Implications
    • Reboredo, S.; Reyes, E.; Vicario, J. L.; Badía, D.; Carrillo, L.; De Cózar, A.; Cossío, F. P. An Amine-Catalyzed Enantioselective [3 + 2] Cycloaddition of Azomethine Ylides and α,β-Unsaturated Aldehydes: Applications and Mechanistic Implications Chem.-Eur. J. 2012, 18, 7179 - 7188
    • (2012) Chem. - Eur. J. , vol.18 , pp. 7179-7188
    • Reboredo, S.1    Reyes, E.2    Vicario, J.L.3    Badía, D.4    Carrillo, L.5    De Cózar, A.6    Cossío, F.P.7
  • 309
    • 84885019661 scopus 로고    scopus 로고
    • A Simple Synthesis of Polysubstituted Pyrrolidines by an Organocatalytic Three-Component Approach Featuring a One-Pot Condensation and [3 + 2]-Cycloaddition Reaction in Aqueous Medium
    • Reboredo, S.; Vicario, J. L.; Carrillo, L.; Reyes, E.; Uria, U. A Simple Synthesis of Polysubstituted Pyrrolidines by an Organocatalytic Three-Component Approach Featuring a One-Pot Condensation and [3 + 2]-Cycloaddition Reaction in Aqueous Medium Synthesis 2013, 2669 - 2678
    • (2013) Synthesis , pp. 2669-2678
    • Reboredo, S.1    Vicario, J.L.2    Carrillo, L.3    Reyes, E.4    Uria, U.5
  • 310
    • 34547682312 scopus 로고    scopus 로고
    • Organocatalytic Asymmetric Multi-Component [C+NC+CC] Synthesis of Highly Functionalized Pyrrolidine Derivatives
    • Ibrahem, I.; Rios, R.; Vesely, J.; Córdova, A. Organocatalytic Asymmetric Multi-Component [C+NC+CC] Synthesis of Highly Functionalized Pyrrolidine Derivatives Tetrahedron Lett. 2007, 48, 6252 - 6257
    • (2007) Tetrahedron Lett. , vol.48 , pp. 6252-6257
    • Ibrahem, I.1    Rios, R.2    Vesely, J.3    Córdova, A.4
  • 311
    • 79961241357 scopus 로고    scopus 로고
    • Dynamic One-Pot Three-Component Catalytic Asymmetric Transformation by Combination of Hydrogen-Bond-Donating and Amine Catalysts
    • Lin, S.; Deiana, L.; Zhao, G. L.; Sun, J.; Córdova, A. Dynamic One-Pot Three-Component Catalytic Asymmetric Transformation by Combination of Hydrogen-Bond-Donating and Amine Catalysts Angew. Chem., Int. Ed. 2011, 50, 7624 - 7630
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 7624-7630
    • Lin, S.1    Deiana, L.2    Zhao, G.L.3    Sun, J.4    Córdova, A.5
  • 312
    • 84255162188 scopus 로고    scopus 로고
    • Complete 2,5-Diastereocontrol in the Organocatalytic Enantioselective [3 + 2] Cycloaddition of Enals with Azomethine Ylides Derived from α-Iminocyanoacetates: Asymmetric Synthesis of Pyrrolidines with Four Stereocentres
    • Reboredo, S.; Vicario, J. L.; Badía, D.; Carrillo, L.; Reyes, E. Complete 2,5-Diastereocontrol in the Organocatalytic Enantioselective [3 + 2] Cycloaddition of Enals with Azomethine Ylides Derived from α-Iminocyanoacetates: Asymmetric Synthesis of Pyrrolidines with Four Stereocentres Adv. Synth. Catal. 2011, 353, 3307 - 3312
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 3307-3312
    • Reboredo, S.1    Vicario, J.L.2    Badía, D.3    Carrillo, L.4    Reyes, E.5
  • 313
    • 84906845813 scopus 로고    scopus 로고
    • Highly Enantioselective Construction of Polycyclic Spirooxindoles by Organocatalytic 1,3-Dipolar Cycloaddition of 2-Cyclohexenone Catalyzed by Proline-Sulfonamide
    • Xiao, J.-A.; Liu, Q.; Ren, J.-W.; Liu, J.; Carter, R. G.; Chen, X.-Q.; Yang, H. Highly Enantioselective Construction of Polycyclic Spirooxindoles by Organocatalytic 1,3-Dipolar Cycloaddition of 2-Cyclohexenone Catalyzed by Proline-Sulfonamide Eur. J. Org. Chem. 2014, 5700 - 5704
    • (2014) Eur. J. Org. Chem. , pp. 5700-5704
    • Xiao, J.-A.1    Liu, Q.2    Ren, J.-W.3    Liu, J.4    Carter, R.G.5    Chen, X.-Q.6    Yang, H.7
  • 314
    • 80755125784 scopus 로고    scopus 로고
    • Organocatalytic Enantioselective (3 + 2) Cycloaddition Using Stable Azomethine Ylides
    • Fernández, N.; Carrillo, L.; Vicario, J. L.; Badía, D.; Reyes, E. Organocatalytic Enantioselective (3 + 2) Cycloaddition Using Stable Azomethine Ylides Chem. Commun. 2011, 47, 12313 - 12315
    • (2011) Chem. Commun. , vol.47 , pp. 12313-12315
    • Fernández, N.1    Carrillo, L.2    Vicario, J.L.3    Badía, D.4    Reyes, E.5
  • 315
    • 37049097154 scopus 로고
    • Brönsted and Lewis Acid Catalysis of X=Y-ZH Cycloadditions
    • Grigg, R.; Gunaratne, H. Q. N. Brönsted and Lewis Acid Catalysis of X=Y-ZH Cycloadditions J. Chem. Soc Chem. Commun. 1982, 384 - 386
    • (1982) J. Chem. Soc. Chem. Commun. , pp. 384-386
    • Grigg, R.1    Gunaratne, H.Q.N.2
  • 316
    • 0001693498 scopus 로고
    • X=Y-ZH Systems as Potential 1.3-Dipoles: Part 14.1 Bronsted and Lewis Acid Catalysis of Cycloadditions of Arylidene Imines of α-Amino Acid Esters
    • Grigg, R.; Gunaratne, H. Q. N.; Sridharan, V. X=Y-ZH Systems as Potential 1.3-Dipoles: Part 14.1 Bronsted and Lewis Acid Catalysis of Cycloadditions of Arylidene Imines of α-Amino Acid Esters Tetrahedron 1987, 43, 5887 - 5898
    • (1987) Tetrahedron , vol.43 , pp. 5887-5898
    • Grigg, R.1    Gunaratne, H.Q.N.2    Sridharan, V.3
  • 317
    • 42649137921 scopus 로고    scopus 로고
    • Asymmetric Organocatalytic Three-Component 1,3-Dipolar Cycloaddition: Control of Stereochemistry via a Chiral Bronsted Acid Activated Dipole
    • Chen, X.-H.; Zhang, W.-Q.; Gong, L.-Z. Asymmetric Organocatalytic Three-Component 1,3-Dipolar Cycloaddition: Control of Stereochemistry via a Chiral Bronsted Acid Activated Dipole J. Am. Chem. Soc. 2008, 130, 5652 - 5653
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 5652-5653
    • Chen, X.-H.1    Zhang, W.-Q.2    Gong, L.-Z.3
  • 318
    • 80052097397 scopus 로고    scopus 로고
    • Binaphthol-Derived Bisphosphoric Acids Serve as Efficient Organocatalysts for Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides to Electron-Deficient Olefins
    • He, L.; Chen, X. H.; Wang, D. N.; Luo, S. W.; Zhang, W. Q.; Yu, J.; Ren, L.; Gong, L. Z. Binaphthol-Derived Bisphosphoric Acids Serve as Efficient Organocatalysts for Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides to Electron-Deficient Olefins J. Am. Chem. Soc. 2011, 133, 13504 - 13518
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 13504-13518
    • He, L.1    Chen, X.H.2    Wang, D.N.3    Luo, S.W.4    Zhang, W.Q.5    Yu, J.6    Ren, L.7    Gong, L.Z.8
  • 319
    • 79955604603 scopus 로고    scopus 로고
    • Asymmetic Organocatalytic 1,3-Dipolar Cycloaddition of Azomethine Ylide to Methyl 2-(2-Nitrophenyl)Acrylate for the Synthesis of Diastereoisomers of Spirotryprostatin A
    • Cheng, M. N.; Wang, H.; Gong, L. Z. Asymmetic Organocatalytic 1,3-Dipolar Cycloaddition of Azomethine Ylide to Methyl 2-(2-Nitrophenyl)Acrylate for the Synthesis of Diastereoisomers of Spirotryprostatin A Org. Lett. 2011, 13, 2418 - 2421
    • (2011) Org. Lett. , vol.13 , pp. 2418-2421
    • Cheng, M.N.1    Wang, H.2    Gong, L.Z.3
  • 320
    • 81255211335 scopus 로고    scopus 로고
    • Bronsted-Acid-Catalyzed Asymmetric Multicomponent Reactions for the Facile Synthesis of Highly Enantioenriched Structurally Diverse Nitrogenous Heterocycles
    • Yu, J.; Shi, F.; Gong, L. Z. Bronsted-Acid-Catalyzed Asymmetric Multicomponent Reactions for the Facile Synthesis of Highly Enantioenriched Structurally Diverse Nitrogenous Heterocycles Acc. Chem. Res. 2011, 44, 1156 - 1171
    • (2011) Acc. Chem. Res. , vol.44 , pp. 1156-1171
    • Yu, J.1    Shi, F.2    Gong, L.Z.3
  • 321
    • 70350676939 scopus 로고    scopus 로고
    • Highly Enantioselective Catalytic 1,3-Dipolar Cycloaddition Involving 2,3-Allenoate Dipolarophiles
    • Yu, J.; He, L.; Chen, X. H.; Song, J.; Chen, W. J.; Gong, L. Z. Highly Enantioselective Catalytic 1,3-Dipolar Cycloaddition Involving 2,3-Allenoate Dipolarophiles Org. Lett. 2009, 11, 4946 - 4949
    • (2009) Org. Lett. , vol.11 , pp. 4946-4949
    • Yu, J.1    He, L.2    Chen, X.H.3    Song, J.4    Chen, W.J.5    Gong, L.Z.6
  • 322
    • 77956581197 scopus 로고    scopus 로고
    • Kinetic Resolution of Racemic 2,3-Allenoates by Organocatalytic Asymmetric 1,3-Dipolar Cycloaddition
    • Yu, J.; Chen, W. J.; Gong, L. Z. Kinetic Resolution of Racemic 2,3-Allenoates by Organocatalytic Asymmetric 1,3-Dipolar Cycloaddition Org. Lett. 2010, 12, 4050 - 4053
    • (2010) Org. Lett. , vol.12 , pp. 4050-4053
    • Yu, J.1    Chen, W.J.2    Gong, L.Z.3
  • 323
    • 84861544403 scopus 로고    scopus 로고
    • Scaffold-Inspired Enantioselective Synthesis of Biologically Important Spiro[pyrrolidin-3,2′-oxindoles] with Structural Diversity through Catalytic Isatin-Derived 1,3-Dipolar Cycloadditions
    • Shi, F.; Tao, Z. L.; Luo, S. W.; Tu, S. J.; Gong, L. Z. Scaffold-Inspired Enantioselective Synthesis of Biologically Important Spiro[pyrrolidin-3,2′-oxindoles] with Structural Diversity through Catalytic Isatin-Derived 1,3-Dipolar Cycloadditions Chem.-Eur. J. 2012, 18, 6885 - 6894
    • (2012) Chem. - Eur. J. , vol.18 , pp. 6885-6894
    • Shi, F.1    Tao, Z.L.2    Luo, S.W.3    Tu, S.J.4    Gong, L.Z.5
  • 324
    • 84879219663 scopus 로고    scopus 로고
    • Biomimetic Asymmetric 1,3-Dioplar Cycloaddition: Amino Acid Precursors in Biosynthesis Serve as Latent Azomethine Ylides
    • Guo, C.; Song, J.; Gong, L. Z. Biomimetic Asymmetric 1,3-Dioplar Cycloaddition: Amino Acid Precursors in Biosynthesis Serve as Latent Azomethine Ylides Org. Lett. 2013, 15, 2676 - 2679
    • (2013) Org. Lett. , vol.15 , pp. 2676-2679
    • Guo, C.1    Song, J.2    Gong, L.Z.3
  • 325
    • 70349742473 scopus 로고    scopus 로고
    • Organocatalytic Synthesis of Spiro[pyrrolidin-3,3′-oxindoles] with High Enantiopurity and Structural Diversity
    • Chen, X.-H.; Wei, Q.; Luo, S.-W.; Xiao, H.; Gong, L.-Z. Organocatalytic Synthesis of Spiro[pyrrolidin-3,3′-oxindoles] with High Enantiopurity and Structural Diversity J. Am. Chem. Soc. 2009, 131, 13819 - 13825
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 13819-13825
    • Chen, X.-H.1    Wei, Q.2    Luo, S.-W.3    Xiao, H.4    Gong, L.-Z.5
  • 326
    • 0034647225 scopus 로고    scopus 로고
    • The Asymmetric Total Synthesis of (+)- and (-)-Spirotryprostatin B
    • Sebahar, P. R.; Williams, R. M. The Asymmetric Total Synthesis of (+)- and (-)-Spirotryprostatin B J. Am. Chem. Soc. 2000, 122, 5666 - 5667
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 5666-5667
    • Sebahar, P.R.1    Williams, R.M.2
  • 327
    • 76349096284 scopus 로고    scopus 로고
    • Asymmetric Organocatalytic Formal Double-Arylation of Azomethines for the Synthesis of Highly Enantiomerically Enriched Isoindolines
    • Wang, C.; Chen, X.-H.; Zhou, S.-M.; Gong, L.-Z. Asymmetric Organocatalytic Formal Double-Arylation of Azomethines for the Synthesis of Highly Enantiomerically Enriched Isoindolines Chem. Commun. 2010, 1275 - 1277
    • (2010) Chem. Commun. , pp. 1275-1277
    • Wang, C.1    Chen, X.-H.2    Zhou, S.-M.3    Gong, L.-Z.4
  • 328
    • 61349181405 scopus 로고    scopus 로고
    • Direct Assembly of Aldehydes, Amino Esters, and Anilines into Chiral Imidazolidines via Bronsted Acid Catalyzed Asymmetric 1,3-Dipolar Cycloadditions
    • Liu, W.-J.; Chen, X.-H.; Gong, L.-Z. Direct Assembly of Aldehydes, Amino Esters, and Anilines into Chiral Imidazolidines via Bronsted Acid Catalyzed Asymmetric 1,3-Dipolar Cycloadditions Org. Lett. 2008, 10, 5357 - 5360
    • (2008) Org. Lett. , vol.10 , pp. 5357-5360
    • Liu, W.-J.1    Chen, X.-H.2    Gong, L.-Z.3
  • 329
    • 84899982058 scopus 로고    scopus 로고
    • Catalytic Asymmetric Homo-1,3-Dipolar Cycloadditions of Azomethine Ylides: Diastereo- and Enantioselective Synthesis of Imidazolidines
    • Zhu, R. Y.; Wang, C. S.; Jiang, F.; Shi, F.; Tu, S. J. Catalytic Asymmetric Homo-1,3-Dipolar Cycloadditions of Azomethine Ylides: Diastereo- and Enantioselective Synthesis of Imidazolidines Tetrahedron: Asymmetry 2014, 25, 617 - 624
    • (2014) Tetrahedron: Asymmetry , vol.25 , pp. 617-624
    • Zhu, R.Y.1    Wang, C.S.2    Jiang, F.3    Shi, F.4    Tu, S.J.5
  • 330
    • 80052211267 scopus 로고    scopus 로고
    • The Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Ynones with Azomethine Ylides
    • Shi, F.; Luo, S. W.; Tao, Z. L.; He, L.; Yu, J.; Tu, S. J.; Gong, L. Z. The Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Ynones with Azomethine Ylides Org. Lett. 2011, 13, 4680 - 4683
    • (2011) Org. Lett. , vol.13 , pp. 4680-4683
    • Shi, F.1    Luo, S.W.2    Tao, Z.L.3    He, L.4    Yu, J.5    Tu, S.J.6    Gong, L.Z.7
  • 331
    • 84862966404 scopus 로고    scopus 로고
    • Highly Enantioselective Synthesis of Biologically Important 2,5-Dihydropyrroles via Phosphoric Acid-Catalyzed Three-Component Reactions and Evaluation of their Cytotoxicity
    • Shi, F.; Tao, Z. L.; Yu, J.; Tu, S. J. Highly Enantioselective Synthesis of Biologically Important 2,5-Dihydropyrroles via Phosphoric Acid-Catalyzed Three-Component Reactions and Evaluation of their Cytotoxicity Tetrahedron: Asymmetry 2011, 22, 2056 - 2064
    • (2011) Tetrahedron: Asymmetry , vol.22 , pp. 2056-2064
    • Shi, F.1    Tao, Z.L.2    Yu, J.3    Tu, S.J.4
  • 332
    • 84875852473 scopus 로고    scopus 로고
    • Enantioselective Construction of 2,5-Dihydropyrrole Skeleton with Quaternary Stereogenic Center via Catalytic Asymmetric 1,3-Dipolar Cycloaddition Involving α-Arylglycine Esters
    • Shi, F.; Xing, G. J.; Tan, W.; Zhu, R. Y.; Tu, S. Enantioselective Construction of 2,5-Dihydropyrrole Skeleton with Quaternary Stereogenic Center via Catalytic Asymmetric 1,3-Dipolar Cycloaddition Involving α-Arylglycine Esters Org. Biomol. Chem. 2013, 11, 1482 - 1489
    • (2013) Org. Biomol. Chem. , vol.11 , pp. 1482-1489
    • Shi, F.1    Xing, G.J.2    Tan, W.3    Zhu, R.Y.4    Tu, S.5
  • 333
    • 84884499793 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar Cycloadditions of Alkynes with Isatin-Derived Azomethine Ylides: Enantioselective Synthesis of Spiro[indoline-3,2′-pyrrole] Derivatives
    • Shi, F.; Zhu, R. Y.; Liang, X.; Tu, S. J. Catalytic Asymmetric 1,3-Dipolar Cycloadditions of Alkynes with Isatin-Derived Azomethine Ylides: Enantioselective Synthesis of Spiro[indoline-3,2′-pyrrole] Derivatives Adv. Synth. Catal. 2013, 355, 2447 - 2458
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 2447-2458
    • Shi, F.1    Zhu, R.Y.2    Liang, X.3    Tu, S.J.4
  • 334
    • 84902141798 scopus 로고    scopus 로고
    • Chiral Phosphoric Acid Catalyzed 1,3-Dipolar Cycloadditions of Aldehydes, Diethyl α-Aminomalonate, and Nitroalkenes
    • Luo, W.; Lin, Y.; Yang, D.; He, L. Chiral Phosphoric Acid Catalyzed 1,3-Dipolar Cycloadditions of Aldehydes, Diethyl α-Aminomalonate, and Nitroalkenes Tetrahedron: Asymmetry 2014, 25, 787 - 791
    • (2014) Tetrahedron: Asymmetry , vol.25 , pp. 787-791
    • Luo, W.1    Lin, Y.2    Yang, D.3    He, L.4
  • 335
    • 77951106587 scopus 로고    scopus 로고
    • Organocatalytic Asymmetric Intramolecular [3 + 2] Cycloaddition: A Straightforward Approach to Access Multiply Substituted Hexahydrochromeno[4,3-b] Pyrrolidine Derivatives in High Optical Purity
    • Li, N.; Song, J.; Tu, X. F.; Liu, B.; Chen, X. H.; Gong, L. Z. Organocatalytic Asymmetric Intramolecular [3 + 2] Cycloaddition: A Straightforward Approach to Access Multiply Substituted Hexahydrochromeno[4,3-b] Pyrrolidine Derivatives in High Optical Purity Org. Biomol. Chem. 2010, 8, 2016 - 2019
    • (2010) Org. Biomol. Chem. , vol.8 , pp. 2016-2019
    • Li, N.1    Song, J.2    Tu, X.F.3    Liu, B.4    Chen, X.H.5    Gong, L.Z.6
  • 336
    • 41349123337 scopus 로고    scopus 로고
    • The First Organocatalytic Enantio- and Diastereoselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Nitroalkenes
    • Xue, M.-X.; Zhang, X.-M.; Gong, L.-Z. The First Organocatalytic Enantio- and Diastereoselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Nitroalkenes Synlett 2008, 691 - 694
    • (2008) Synlett , pp. 691-694
    • Xue, M.-X.1    Zhang, X.-M.2    Gong, L.-Z.3
  • 337
    • 56949108837 scopus 로고    scopus 로고
    • Thiourea-Catalyzed Asymmetric Formal [3 + 2] Cycloaddition of Azomethine Ylides with Nitroolefins
    • Xie, J.; Yoshida, K.; Takasu, K.; Takemoto, Y. Thiourea-Catalyzed Asymmetric Formal [3 + 2] Cycloaddition of Azomethine Ylides with Nitroolefins Tetrahedron Lett. 2008, 49, 6910 - 6913
    • (2008) Tetrahedron Lett. , vol.49 , pp. 6910-6913
    • Xie, J.1    Yoshida, K.2    Takasu, K.3    Takemoto, Y.4
  • 338
    • 55449131123 scopus 로고    scopus 로고
    • Reaction Control in the Organocatalytic Asymmetric One-Pot, Three-Component Reaction of Aldehydes, Diethyl α-Aminomalonate and Nitroalkenes: Toward Diversity-Oriented Synthesis
    • Liu, Y. K.; Liu, H.; Du, W.; Yue, L.; Chen, Y. C. Reaction Control in the Organocatalytic Asymmetric One-Pot, Three-Component Reaction of Aldehydes, Diethyl α-Aminomalonate and Nitroalkenes: Toward Diversity-Oriented Synthesis Chem.-Eur. J. 2008, 14, 9873 - 9877
    • (2008) Chem. - Eur. J. , vol.14 , pp. 9873-9877
    • Liu, Y.K.1    Liu, H.2    Du, W.3    Yue, L.4    Chen, Y.C.5
  • 339
    • 79961155855 scopus 로고    scopus 로고
    • Metal-Free Asymmetric 1,3-Dipolar Cycloaddition of N-Arylmaleimides to Azomethine Ylides Catalyzed by Chiral Tertiary Amine Thiourea
    • Bai, J. F.; Wang, L. L.; Peng, L.; Guo, Y. L.; Ming, J. N.; Wang, F. Y.; Xu, X. Y.; Wang, L. X. Metal-Free Asymmetric 1,3-Dipolar Cycloaddition of N-Arylmaleimides to Azomethine Ylides Catalyzed by Chiral Tertiary Amine Thiourea Eur. J. Org. Chem. 2011, 4472 - 4478
    • (2011) Eur. J. Org. Chem. , pp. 4472-4478
    • Bai, J.F.1    Wang, L.L.2    Peng, L.3    Guo, Y.L.4    Ming, J.N.5    Wang, F.Y.6    Xu, X.Y.7    Wang, L.X.8
  • 340
    • 84882411324 scopus 로고    scopus 로고
    • Organocatalytic Diastereo- and Enantioselective 1,3-Dipolar Cycloaddition of Azlactones and Methyleneindolinones
    • Sun, W.; Zhu, G.; Wu, C.; Li, G.; Hong, L.; Wang, R. Organocatalytic Diastereo- and Enantioselective 1,3-Dipolar Cycloaddition of Azlactones and Methyleneindolinones Angew. Chem., Int. Ed. 2013, 52, 8633 - 8637
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 8633-8637
    • Sun, W.1    Zhu, G.2    Wu, C.3    Li, G.4    Hong, L.5    Wang, R.6
  • 341
    • 84876530424 scopus 로고    scopus 로고
    • Efficient Construction of Highly Functionalized Spiro[γ-butyrolactone-pyrrolidin-3,3′-oxindole] Tricyclic Skeletons via an Organocatalytic 1,3-Dipolar Cycloaddition
    • Wang, L.; Shi, X. M.; Dong, W. P.; Zhu, L. P.; Wang, R. Efficient Construction of Highly Functionalized Spiro[γ-butyrolactone-pyrrolidin-3,3′-oxindole] Tricyclic Skeletons via an Organocatalytic 1,3-Dipolar Cycloaddition Chem. Commun. 2013, 49, 3458 - 3460
    • (2013) Chem. Commun. , vol.49 , pp. 3458-3460
    • Wang, L.1    Shi, X.M.2    Dong, W.P.3    Zhu, L.P.4    Wang, R.5
  • 342
    • 67649382042 scopus 로고    scopus 로고
    • Acid-Base Dual-Functional Catalysis by Axially Chiral Guanidine in Enantioselective [3 + 2] Cycloaddition of Maleate to Schiff Bases as a Precursor of Azomethine Ylides
    • Nakano, M.; Terada, M. Acid-Base Dual-Functional Catalysis by Axially Chiral Guanidine in Enantioselective [3 + 2] Cycloaddition of Maleate to Schiff Bases as a Precursor of Azomethine Ylides Synlett 2009, 1670 - 1674
    • (2009) Synlett , pp. 1670-1674
    • Nakano, M.1    Terada, M.2
  • 343
    • 84907710391 scopus 로고    scopus 로고
    • Highly Stereoselective Synthesis of Functionalized Pyrrolo[3,2-c]quinolines via N-Heterocyclic Carbene Catalyzed Cascade Sequence
    • Yang, Y.-J.; Zhang, H.-R.; Zhu, S.-Y.; Zhu, P.; Hui, X.-P. Highly Stereoselective Synthesis of Functionalized Pyrrolo[3,2-c]quinolines via N-Heterocyclic Carbene Catalyzed Cascade Sequence Org. Lett. 2014, 16, 5048 - 5051
    • (2014) Org. Lett. , vol.16 , pp. 5048-5051
    • Yang, Y.-J.1    Zhang, H.-R.2    Zhu, S.-Y.3    Zhu, P.4    Hui, X.-P.5
  • 344
    • 33847086314 scopus 로고
    • A Particularly Convenient Preparation of Benzohydroximinoyl Chlorides (Nitrile Oxide Precursors)
    • Liu, K.-C.; Shelton, B. R.; Howe, R. K. A Particularly Convenient Preparation of Benzohydroximinoyl Chlorides (Nitrile Oxide Precursors) J. Org. Chem. 1980, 45, 3916 - 3918
    • (1980) J. Org. Chem. , vol.45 , pp. 3916-3918
    • Liu, K.-C.1    Shelton, B.R.2    Howe, R.K.3
  • 345
    • 0001352454 scopus 로고
    • The Reactions of Primary Nitroparaffins with Isocyanates
    • Mukaiyama, T.; Hoshino, T. The Reactions of Primary Nitroparaffins with Isocyanates J. Am. Chem. Soc. 1960, 82, 5339 - 5342
    • (1960) J. Am. Chem. Soc. , vol.82 , pp. 5339-5342
    • Mukaiyama, T.1    Hoshino, T.2
  • 346
    • 0001133546 scopus 로고
    • Nitrile Oxides. V. Stable Aromatic Nitrile Oxides
    • Grundmann, C.; Dean, J. M. Nitrile Oxides. V. Stable Aromatic Nitrile Oxides J. Org. Chem. 1965, 30, 2809 - 2812
    • (1965) J. Org. Chem. , vol.30 , pp. 2809-2812
    • Grundmann, C.1    Dean, J.M.2
  • 347
    • 0037459877 scopus 로고    scopus 로고
    • Amine-Promoted Cyclocondensation of Highly Substituted Aromatic Nitrile Oxides with Diketones
    • Bode, J. W.; Hachisu, Y.; Matsuura, T.; Suzuki, K. Amine-Promoted Cyclocondensation of Highly Substituted Aromatic Nitrile Oxides with Diketones Tetrahedron Lett. 2003, 44, 3555 - 3558
    • (2003) Tetrahedron Lett. , vol.44 , pp. 3555-3558
    • Bode, J.W.1    Hachisu, Y.2    Matsuura, T.3    Suzuki, K.4
  • 348
    • 0000930644 scopus 로고
    • First Successful Metal Coordination Control in 1,3-Dipolar Cycloadditions. High-Rate Acceleration and Regio- and Stereocontrol of Nitrile Oxide Cycloadditions to the Magnesium Alkoxides of Allylic and Homoallylic Alcohols
    • Kanemasa, S.; Nishiuchi, M.; Kamimura, A.; Hori, K. First Successful Metal Coordination Control in 1,3-Dipolar Cycloadditions. High-Rate Acceleration and Regio- and Stereocontrol of Nitrile Oxide Cycloadditions to the Magnesium Alkoxides of Allylic and Homoallylic Alcohols J. Am. Chem. Soc. 1994, 116, 2324 - 2339
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 2324-2339
    • Kanemasa, S.1    Nishiuchi, M.2    Kamimura, A.3    Hori, K.4
  • 349
    • 0034829891 scopus 로고    scopus 로고
    • Stereoselective Syntheses of Epothilones A and B via Directed Nitrile Oxide Cycloaddition
    • Bode, J. W.; Carreira, E. M. Stereoselective Syntheses of Epothilones A and B via Directed Nitrile Oxide Cycloaddition J. Am. Chem. Soc. 2001, 123, 3611 - 3612
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 3611-3612
    • Bode, J.W.1    Carreira, E.M.2
  • 350
    • 0035929443 scopus 로고    scopus 로고
    • Stereoselective Syntheses of Epothilones A and B via Nitrile Oxide Cycloadditions and Related Studies
    • Bode, J. W.; Carreira, E. M. Stereoselective Syntheses of Epothilones A and B via Nitrile Oxide Cycloadditions and Related Studies J. Org. Chem. 2001, 66, 6410 - 6424
    • (2001) J. Org. Chem. , vol.66 , pp. 6410-6424
    • Bode, J.W.1    Carreira, E.M.2
  • 351
    • 0001386311 scopus 로고    scopus 로고
    • A General Solution to the Modular Synthesis of Polyketide Building Blocks by Kanemasa Hydroxy-Directed Nitrile Oxide Cycloadditions
    • Bode, J. W.; Fraefel, N.; Muri, D.; Carreira, E. M. A General Solution to the Modular Synthesis of Polyketide Building Blocks by Kanemasa Hydroxy-Directed Nitrile Oxide Cycloadditions Angew. Chem., Int. Ed. 2001, 40, 2082 - 2085
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 2082-2085
    • Bode, J.W.1    Fraefel, N.2    Muri, D.3    Carreira, E.M.4
  • 352
    • 0002803192 scopus 로고
    • Enantioselective Synthesis of 2-Isoxazolines via Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxide to Achiral Allyl Alcohol
    • Ukaji, Y.; Sada, K.; Inomata, K. Enantioselective Synthesis of 2-Isoxazolines via Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxide to Achiral Allyl Alcohol Chem. Lett. 1993, 22, 1847 - 1850
    • (1993) Chem. Lett. , vol.22 , pp. 1847-1850
    • Ukaji, Y.1    Sada, K.2    Inomata, K.3
  • 353
    • 0030500933 scopus 로고    scopus 로고
    • Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides to an Achiral Allyl Alcohol Utilizing Diisopropyl Tartrate as a Chiral Auxiliary
    • Shimizu, M.; Ukaji, Y.; Inomata, K. Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides to an Achiral Allyl Alcohol Utilizing Diisopropyl Tartrate as a Chiral Auxiliary Chem. Lett. 1996, 25, 455 - 456
    • (1996) Chem. Lett. , vol.25 , pp. 455-456
    • Shimizu, M.1    Ukaji, Y.2    Inomata, K.3
  • 354
    • 0000705574 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides to γ-Substituted Allylic Alcohols
    • Yoshida, Y.; Ukaji, Y.; Fujinami, S.; Inomata, K. Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides to γ-Substituted Allylic Alcohols Chem. Lett. 1998, 27, 1023 - 1024
    • (1998) Chem. Lett. , vol.27 , pp. 1023-1024
    • Yoshida, Y.1    Ukaji, Y.2    Fujinami, S.3    Inomata, K.4
  • 355
    • 0037027697 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides Generated in situ by Direct Oxidation of Aldoximes
    • Tsuji, M.; Ukaji, Y.; Inomata, K. Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides Generated in situ by Direct Oxidation of Aldoximes Chem. Lett. 2002, 31, 1112 - 1113
    • (2002) Chem. Lett. , vol.31 , pp. 1112-1113
    • Tsuji, M.1    Ukaji, Y.2    Inomata, K.3
  • 356
    • 0038729635 scopus 로고    scopus 로고
    • Development of New Asymmetric Reactions Utilizing Tartaric Acid Esters as Chiral Auxiliaries. The Design of an Efficient Chiral Multinucleating System
    • Ukaji, Y.; Inomata, K. Development of New Asymmetric Reactions Utilizing Tartaric Acid Esters as Chiral Auxiliaries. The Design of an Efficient Chiral Multinucleating System Synlett 2003, 1075 - 1087
    • (2003) Synlett , pp. 1075-1087
    • Ukaji, Y.1    Inomata, K.2
  • 357
    • 38949101467 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition Reactions Using Complexes of (-)-Sparteine
    • Gucma, M.; Golebiewski, W. M. Enantioselective 1,3-Dipolar Cycloaddition Reactions Using Complexes of (-)-Sparteine J. Heterocycl. Chem. 2008, 45, 241 - 245
    • (2008) J. Heterocycl. Chem. , vol.45 , pp. 241-245
    • Gucma, M.1    Golebiewski, W.M.2
  • 358
    • 2342633120 scopus 로고    scopus 로고
    • Chiral Lewis Acid Catalysis in Nitrile Oxide Cycloadditions
    • Sibi, M. P.; Itoh, K.; Jasperse, C. P. Chiral Lewis Acid Catalysis in Nitrile Oxide Cycloadditions J. Am. Chem. Soc. 2004, 126, 5366 - 5367
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5366-5367
    • Sibi, M.P.1    Itoh, K.2    Jasperse, C.P.3
  • 360
    • 0006465448 scopus 로고
    • 1,3-Dipolar Cycloaddition: Molecular Sieves Assisted Generation of Nitrile Oxides from Hydroximoyl Chlorides
    • Kim, J. N.; Ryu, E. K. 1,3-Dipolar Cycloaddition: Molecular Sieves Assisted Generation of Nitrile Oxides from Hydroximoyl Chlorides Heterocycles 1990, 31, 1693 - 1697
    • (1990) Heterocycles , vol.31 , pp. 1693-1697
    • Kim, J.N.1    Ryu, E.K.2
  • 361
    • 64549123539 scopus 로고    scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition Reactions of Nitrile Oxides Catalyzed by Chiral Binaphthyldiimine-Ni(II) Complexes
    • Suga, H.; Adachi, Y.; Fujimoto, K.; Furihata, Y.; Tsuchida, T.; Kakehi, A.; Baba, T. Asymmetric 1,3-Dipolar Cycloaddition Reactions of Nitrile Oxides Catalyzed by Chiral Binaphthyldiimine-Ni(II) Complexes J. Org. Chem. 2009, 74, 1099 - 1113
    • (2009) J. Org. Chem. , vol.74 , pp. 1099-1113
    • Suga, H.1    Adachi, Y.2    Fujimoto, K.3    Furihata, Y.4    Tsuchida, T.5    Kakehi, A.6    Baba, T.7
  • 363
    • 84906086444 scopus 로고    scopus 로고
    • Asymmetric Synthesis of Spiro[isoxazolin-3,3′-oxindoles] via the Catalytic 1,3-Dipolar Cycloaddition Reaction of Nitrile Oxides
    • Lian, X.; Guo, S.; Wang, G.; Lin, L.; Liu, X.; Feng, X. Asymmetric Synthesis of Spiro[isoxazolin-3,3′-oxindoles] via the Catalytic 1,3-Dipolar Cycloaddition Reaction of Nitrile Oxides J. Org. Chem. 2014, 79, 7703 - 7710
    • (2014) J. Org. Chem. , vol.79 , pp. 7703-7710
    • Lian, X.1    Guo, S.2    Wang, G.3    Lin, L.4    Liu, X.5    Feng, X.6
  • 364
    • 20444457507 scopus 로고    scopus 로고
    • An Entry to a Chiral Dihydropyrazole Scaffold: Enantioselective [3 + 2] Cycloaddition of Nitrile Imines
    • Sibi, M. P.; Stanley, L. M.; Jasperse, C. P. An Entry to a Chiral Dihydropyrazole Scaffold: Enantioselective [3 + 2] Cycloaddition of Nitrile Imines J. Am. Chem. Soc. 2005, 127, 8276 - 8277
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 8276-8277
    • Sibi, M.P.1    Stanley, L.M.2    Jasperse, C.P.3
  • 365
    • 33845254820 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition of Nitrile Imines to α-Substituted and α,β-Disubstituted α,β-Unsaturated Carbonyl Substrates: A Method for Synthesizing Dihydropyrazoles Bearing a Chiral Quaternary Center
    • Sibi, M. P.; Stanley, L. M.; Soeta, T. Enantioselective 1,3-Dipolar Cycloaddition of Nitrile Imines to α-Substituted and α,β-Disubstituted α,β-Unsaturated Carbonyl Substrates: A Method for Synthesizing Dihydropyrazoles Bearing a Chiral Quaternary Center Adv. Synth. Catal. 2006, 348, 2371 - 2375
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 2371-2375
    • Sibi, M.P.1    Stanley, L.M.2    Soeta, T.3
  • 366
    • 84874045843 scopus 로고    scopus 로고
    • Asymmetric Catalytic 1,3-Dipolar Cycloaddition Reaction of Nitrile Imines for the Synthesis of Chiral Spiro-Pyrazoline-Oxindoles
    • Wang, G.; Liu, X.; Huang, T.; Kuang, Y.; Lin, L.; Feng, X. Asymmetric Catalytic 1,3-Dipolar Cycloaddition Reaction of Nitrile Imines for the Synthesis of Chiral Spiro-Pyrazoline-Oxindoles Org. Lett. 2013, 15, 76 - 79
    • (2013) Org. Lett. , vol.15 , pp. 76-79
    • Wang, G.1    Liu, X.2    Huang, T.3    Kuang, Y.4    Lin, L.5    Feng, X.6
  • 367
    • 84886834909 scopus 로고    scopus 로고
    • Catalytic, Enantioselective 1,3-Dipolar Cycloadditions of Nitrile Imines with Methyleneindolinones
    • Gerten, A. L.; Slade, M. C.; Pugh, K. M.; Stanley, L. M. Catalytic, Enantioselective 1,3-Dipolar Cycloadditions of Nitrile Imines with Methyleneindolinones Org. Biomol. Chem. 2013, 11, 7834 - 7837
    • (2013) Org. Biomol. Chem. , vol.11 , pp. 7834-7837
    • Gerten, A.L.1    Slade, M.C.2    Pugh, K.M.3    Stanley, L.M.4
  • 368
    • 72449144105 scopus 로고    scopus 로고
    • Diastereoselective Cycloadditions Using Chiral Oxzolidinones without Lewis Acid
    • Sibi, M. P.; Soeta, T.; Jasperse, C. P. Diastereoselective Cycloadditions Using Chiral Oxzolidinones without Lewis Acid Org. Lett. 2009, 11, 5366 - 5369
    • (2009) Org. Lett. , vol.11 , pp. 5366-5369
    • Sibi, M.P.1    Soeta, T.2    Jasperse, C.P.3
  • 369
    • 0039025553 scopus 로고
    • Electrocyclic Ring Opening Reactions of Ethylene Oxides
    • Husingen, R. Electrocyclic Ring Opening Reactions of Ethylene Oxides Angew. Chem., Int. Ed. 1977, 16, 572 - 585
    • (1977) Angew. Chem., Int. Ed. , vol.16 , pp. 572-585
    • Husingen, R.1
  • 370
    • 0000100584 scopus 로고    scopus 로고
    • Recent Advances in Asymmetric Catalytic Metal Carbene Transformations
    • Doyle, M. P.; Forbes, D. C. Recent Advances in Asymmetric Catalytic Metal Carbene Transformations Chem. Rev. 1998, 98, 911 - 936
    • (1998) Chem. Rev. , vol.98 , pp. 911-936
    • Doyle, M.P.1    Forbes, D.C.2
  • 371
    • 57249093643 scopus 로고    scopus 로고
    • Catalytic Enantioselective Rearrangements and Cycloadditions Involving Ylides from Diazo Compounds
    • Hodgson, D. M.; Pierard, F. Y. T. M.; Stupple, P. A. Catalytic Enantioselective Rearrangements and Cycloadditions Involving Ylides from Diazo Compounds Chem. Soc. Rev. 2001, 30, 50 - 61
    • (2001) Chem. Soc. Rev. , vol.30 , pp. 50-61
    • Hodgson, D.M.1    Pierard, F.Y.T.M.2    Stupple, P.A.3
  • 372
    • 0037131941 scopus 로고    scopus 로고
    • Tandem Cyclization-Cycloaddition Reactions of Rhodium Generated Carbenoids from α-Diazo Carbonyl Compounds
    • Mehta, G.; Muthusamy, S. Tandem Cyclization-Cycloaddition Reactions of Rhodium Generated Carbenoids from α-Diazo Carbonyl Compounds Tetrahedron 2002, 58, 9477 - 9504
    • (2002) Tetrahedron , vol.58 , pp. 9477-9504
    • Mehta, G.1    Muthusamy, S.2
  • 373
    • 22144466526 scopus 로고    scopus 로고
    • Application of the Carbene Cyclization-Cycloaddition Cascade in Total Synthesis
    • Chiu, P. Application of the Carbene Cyclization-Cycloaddition Cascade in Total Synthesis Pure Appl. Chem. 2005, 77, 1183 - 1189
    • (2005) Pure Appl. Chem. , vol.77 , pp. 1183-1189
    • Chiu, P.1
  • 374
    • 27744433520 scopus 로고    scopus 로고
    • The Interaction of Rhodium Carbenoids with Carbonyl Compounds as a Method for the Synthesis of Tetrahydrofurans
    • Padwa, A. The Interaction of Rhodium Carbenoids with Carbonyl Compounds as a Method for the Synthesis of Tetrahydrofurans J. Organomet. Chem. 2005, 690, 5533 - 5540
    • (2005) J. Organomet. Chem. , vol.690 , pp. 5533-5540
    • Padwa, A.1
  • 375
    • 39949084476 scopus 로고    scopus 로고
    • Cycloaddition of Oxidopyrylium Species in Organic Synthesis
    • Singh, V.; Murali Krishna, U.; Vikrant Trivedi, G. K. Cycloaddition of Oxidopyrylium Species in Organic Synthesis Tetrahedron 2008, 64, 3405 - 3428
    • (2008) Tetrahedron , vol.64 , pp. 3405-3428
    • Singh, V.1    Murali Krishna, U.2    Vikrant Trivedi, G.K.3
  • 376
    • 80052932651 scopus 로고    scopus 로고
    • Intramolecular Cycloaddition of Carbonyl Ylides as a Strategy for Natural Product Synthesis
    • Padwa, A. Intramolecular Cycloaddition of Carbonyl Ylides as a Strategy for Natural Product Synthesis Tetrahedron 2011, 67, 8057 - 8072
    • (2011) Tetrahedron , vol.67 , pp. 8057-8072
    • Padwa, A.1
  • 377
    • 0001410289 scopus 로고
    • Formation and Reaction of Carbonyl Ylides. Production of 2:1-Cydoadducts of 2-Benzopyrylium-4-olates with Carbonyl Compounds
    • Ibata, T.; Toyoda, J. Formation and Reaction of Carbonyl Ylides. Production of 2:1-Cydoadducts of 2-Benzopyrylium-4-olates with Carbonyl Compounds Bull. Chem. Soc. Jpn. 1986, 59, 2489 - 2493 and references therein.
    • (1986) Bull. Chem. Soc. Jpn. , vol.59 , pp. 2489-2493
    • Ibata, T.1    Toyoda, J.2
  • 378
    • 0038094260 scopus 로고
    • Generation and Utilization of Carbonyl Ylides via the Tandem Cyclization-Cycloaddition Method
    • Padwa, A. Generation and Utilization of Carbonyl Ylides via the Tandem Cyclization-Cycloaddition Method Acc. Chem. Res. 1991, 24, 22 - 28
    • (1991) Acc. Chem. Res. , vol.24 , pp. 22-28
    • Padwa, A.1
  • 379
    • 0000936734 scopus 로고
    • Ylide Formation from the Reaction of Carbenes and Carbenoids with Heteroatom Lone Pairs
    • Padwa, A.; Hornbuckle, S. F. Ylide Formation from the Reaction of Carbenes and Carbenoids with Heteroatom Lone Pairs Chem. Rev. 1991, 91, 263 - 309
    • (1991) Chem. Rev. , vol.91 , pp. 263-309
    • Padwa, A.1    Hornbuckle, S.F.2
  • 380
    • 0000550687 scopus 로고    scopus 로고
    • Cascade Processes of Metallo Carbenoids
    • Padwa, A.; Weingarten, M. D. Cascade Processes of Metallo Carbenoids Chem. Rev. 1996, 96, 223 - 270
    • (1996) Chem. Rev. , vol.96 , pp. 223-270
    • Padwa, A.1    Weingarten, M.D.2
  • 381
    • 0002647908 scopus 로고    scopus 로고
    • The Domino Cycloaddition/N-Acyliminium Ion Cyclization Cascade
    • Padwa, A. The Domino Cycloaddition/N-Acyliminium Ion Cyclization Cascade Chem. Commun. 1998, 1417 - 1424
    • (1998) Chem. Commun. , pp. 1417-1424
    • Padwa, A.1
  • 382
    • 22144484538 scopus 로고    scopus 로고
    • Catalytic Decomposition of Diazo Compounds as a Method for Generating Carbonyl-Ylide Dipoles
    • Padwa, A. Catalytic Decomposition of Diazo Compounds as a Method for Generating Carbonyl-Ylide Dipoles Helv. Chim. Acta 2005, 88, 1357 - 1374
    • (2005) Helv. Chim. Acta , vol.88 , pp. 1357-1374
    • Padwa, A.1
  • 383
    • 0001765361 scopus 로고    scopus 로고
    • Stereocontrol in Intermolecular Dirhodium(II)-Catalyzed Carbonyl Ylide Formation and Reactions. Dioxolanes and Dihydrofurans
    • Doyle, M. P.; Forbes, D. C.; Protopopova, M. N.; Stanley, S. A.; Vasbinder, M. M.; Xavier, K. R. Stereocontrol in Intermolecular Dirhodium(II)-Catalyzed Carbonyl Ylide Formation and Reactions. Dioxolanes and Dihydrofurans J. Org. Chem. 1997, 62, 7210 - 7215
    • (1997) J. Org. Chem. , vol.62 , pp. 7210-7215
    • Doyle, M.P.1    Forbes, D.C.2    Protopopova, M.N.3    Stanley, S.A.4    Vasbinder, M.M.5    Xavier, K.R.6
  • 384
    • 0030840478 scopus 로고    scopus 로고
    • Catalytic Enantioselective Tandem Carbonyl Ylide Formation-Cycloaddition
    • Hodgson, D. M.; Stupple, P. A.; Johnstone, C. Catalytic Enantioselective Tandem Carbonyl Ylide Formation-Cycloaddition Tetrahedron Lett. 1997, 38, 6471 - 6472
    • (1997) Tetrahedron Lett. , vol.38 , pp. 6471-6472
    • Hodgson, D.M.1    Stupple, P.A.2    Johnstone, C.3
  • 386
    • 65549106304 scopus 로고    scopus 로고
    • Catalytic Enantioselective Tandem Carbonyl Ylide Formation-Intramolecular Cycloaddition with Unsaturated α-Diazo-β,ε-Diketo Sulfones
    • Hodgson, D. M.; Glen, R.; Redgrave, A. J. Catalytic Enantioselective Tandem Carbonyl Ylide Formation-Intramolecular Cycloaddition with Unsaturated α-Diazo-β,ε-Diketo Sulfones Tetrahedron: Asymmetry 2009, 20, 754 - 757.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 754-757
    • Hodgson, D.M.1    Glen, R.2    Redgrave, A.J.3
  • 387
    • 0026727764 scopus 로고
    • Rhodium (II) Catalyzed Intramolecular Dipolar Cycloaddition Reactions of Carbonyl Ylides. Computational and Empirical Studies of the Regio- and Chemoselective Effect of Catalyst Ligand
    • Padwa, A.; Austin, D. J.; Hornbuckle, S. F.; Price, A. T. Rhodium (II) Catalyzed Intramolecular Dipolar Cycloaddition Reactions of Carbonyl Ylides. Computational and Empirical Studies of the Regio- and Chemoselective Effect of Catalyst Ligand Tetrahedron Lett. 1992, 33, 6427 - 6430
    • (1992) Tetrahedron Lett. , vol.33 , pp. 6427-6430
    • Padwa, A.1    Austin, D.J.2    Hornbuckle, S.F.3    Price, A.T.4
  • 388
    • 0002723024 scopus 로고    scopus 로고
    • Ligand-Induced Selectivity in the Rhodium(II)-Catalyzed Reactions of α-Diazo Carbonyl Compounds
    • Padwa, A.; Austin, D. J.; Hornbuckle, S. F. Ligand-Induced Selectivity in the Rhodium(II)-Catalyzed Reactions of α-Diazo Carbonyl Compounds J. Org. Chem. 1996, 61, 63 - 72
    • (1996) J. Org. Chem. , vol.61 , pp. 63-72
    • Padwa, A.1    Austin, D.J.2    Hornbuckle, S.F.3
  • 389
    • 0037140888 scopus 로고    scopus 로고
    • [3 + 2] Cycloaddition Reactions of Arylacetylenes with Carbonyl Ylides Derived from 1-Aryl-1-diazohexane-2,5-diones
    • Hodgson, D. M.; Glen, R.; Redgrave, A. J. [3 + 2] Cycloaddition Reactions of Arylacetylenes with Carbonyl Ylides Derived from 1-Aryl-1-diazohexane-2,5-diones Tetrahedron Lett. 2002, 43, 3927 - 3930
    • (2002) Tetrahedron Lett. , vol.43 , pp. 3927-3930
    • Hodgson, D.M.1    Glen, R.2    Redgrave, A.J.3
  • 390
    • 0037418808 scopus 로고    scopus 로고
    • Catalytic Enantioselective Intermolecular Cycloadditions of a 2-Diazo-3,6-diketoester-Derived Carbonyl Ylide with Alkyne and Strained Alkene Dipolarophiles
    • Hodgson, D. M.; Labande, A. H.; Glen, R.; Redgrave, A. J. Catalytic Enantioselective Intermolecular Cycloadditions of a 2-Diazo-3,6-diketoester-Derived Carbonyl Ylide with Alkyne and Strained Alkene Dipolarophiles Tetrahedron: Asymmetry 2003, 14, 921 - 924
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 921-924
    • Hodgson, D.M.1    Labande, A.H.2    Glen, R.3    Redgrave, A.J.4
  • 391
    • 1842631435 scopus 로고    scopus 로고
    • Catalytic Enantioselective Intermolecular Cycloadditions of 2-Diazo-3,6-diketoester-Derived Carbonyl Ylides with Alkene Dipolarophiles
    • Hodgson, D. M.; Brückl, T.; Glen, R.; Labande, A. H.; Selden, D. A.; Dossetter, A. G.; Redgrave, A. J. Catalytic Enantioselective Intermolecular Cycloadditions of 2-Diazo-3,6-diketoester-Derived Carbonyl Ylides with Alkene Dipolarophiles Proc. Natl. Acad. Sci. U.S.A. 2004, 101, 5450 - 5454
    • (2004) Proc. Natl. Acad. Sci. U.S.A. , vol.101 , pp. 5450-5454
    • Hodgson, D.M.1    Brückl, T.2    Glen, R.3    Labande, A.H.4    Selden, D.A.5    Dossetter, A.G.6    Redgrave, A.J.7
  • 392
    • 0032516374 scopus 로고    scopus 로고
    • Stereocontrol of Metal-Catalyzed Cycloaddition of Carbonyl Ylide with N-Substituted Maleimide
    • Suga, H.; Ishida, H.; Ibata, T. Stereocontrol of Metal-Catalyzed Cycloaddition of Carbonyl Ylide with N-Substituted Maleimide Tetrahedron Lett. 1998, 39, 3165 - 3166
    • (1998) Tetrahedron Lett. , vol.39 , pp. 3165-3166
    • Suga, H.1    Ishida, H.2    Ibata, T.3
  • 393
    • 0033576992 scopus 로고    scopus 로고
    • Enantiocontrol in Tandem Carbonyl Ylide Formation and Intermolecular 1,3-Dipolar Cycloaddition of α-Diazo Ketones Mediated by Chiral Dirhodium(II) Carboxylate Catalyst
    • Kitagaki, S.; Anada, M.; Kataoka, O.; Matsuno, K.; Umeda, C.; Watanabe, N.; Hashimoto, S. Enantiocontrol in Tandem Carbonyl Ylide Formation and Intermolecular 1,3-Dipolar Cycloaddition of α-Diazo Ketones Mediated by Chiral Dirhodium(II) Carboxylate Catalyst J. Am. Chem. Soc. 1999, 121, 1417 - 1418
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 1417-1418
    • Kitagaki, S.1    Anada, M.2    Kataoka, O.3    Matsuno, K.4    Umeda, C.5    Watanabe, N.6    Hashimoto, S.7
  • 394
    • 0027209354 scopus 로고
    • Enhancement of Enantioselectivity in Intramolecular C-H Insertion Reactions of α-Diazo β-Keto Esters Catalyzed by Chiral Dirhodium(II) Carboxylates
    • Hashimoto, S.-I.; Watanabe, N.; Sato, T.; Shiro, M.; Ikegami, S. Enhancement of Enantioselectivity in Intramolecular C-H Insertion Reactions of α-Diazo β-Keto Esters Catalyzed by Chiral Dirhodium(II) Carboxylates Tetrahedron Lett. 1993, 34, 5109 - 5112
    • (1993) Tetrahedron Lett. , vol.34 , pp. 5109-5112
    • Hashimoto, S.-I.1    Watanabe, N.2    Sato, T.3    Shiro, M.4    Ikegami, S.5
  • 395
    • 0034730008 scopus 로고    scopus 로고
    • Enantioselective Intermolecular 1,3-Dipolar Cycloaddition via Ester-Derived Carbonyl Ylide Formation Catalyzed by Chiral Dirhodium(II) Carboxylates
    • Kitagaki, S.; Yasugahira, M.; Anada, M.; Nakajima, M.; Hashimoto, S. Enantioselective Intermolecular 1,3-Dipolar Cycloaddition via Ester-Derived Carbonyl Ylide Formation Catalyzed by Chiral Dirhodium(II) Carboxylates Tetrahedron Lett. 2000, 41, 5931 - 5935
    • (2000) Tetrahedron Lett. , vol.41 , pp. 5931-5935
    • Kitagaki, S.1    Yasugahira, M.2    Anada, M.3    Nakajima, M.4    Hashimoto, S.5
  • 396
    • 54049087840 scopus 로고    scopus 로고
    • Catalytic Enantioselective Intermolecular Cycloaddition of 2-Diazo-3,6-diketoester-Derived Carbonyl Ylides with Alkynes and Styrenes Using Chiral Dirhodium(II) Carboxylates
    • Shimada, N.; Anada, M.; Nakamura, S.; Nambu, H.; Tsutsui, H.; Hashimoto, S. Catalytic Enantioselective Intermolecular Cycloaddition of 2-Diazo-3,6-diketoester-Derived Carbonyl Ylides with Alkynes and Styrenes Using Chiral Dirhodium(II) Carboxylates Org. Lett. 2008, 10, 3603 - 3606
    • (2008) Org. Lett. , vol.10 , pp. 3603-3606
    • Shimada, N.1    Anada, M.2    Nakamura, S.3    Nambu, H.4    Tsutsui, H.5    Hashimoto, S.6
  • 399
    • 65549146503 scopus 로고    scopus 로고
    • Asymmetric Approach to the Pentacyclic Skeleton of Aspidosperma Alkaloids via Enantioselective Intramolecular 1,3-Dipolar Cycloaddition of Carbonyl Ylides Catalyzed by Chiral Dirhodium(II) Carboxylates
    • Nambu, H.; Hikime, M.; Krishnamurthi, J.; Kamiya, M.; Shimada, N.; Hashimoto, S. Asymmetric Approach to the Pentacyclic Skeleton of Aspidosperma Alkaloids via Enantioselective Intramolecular 1,3-Dipolar Cycloaddition of Carbonyl Ylides Catalyzed by Chiral Dirhodium(II) Carboxylates Tetrahedron Lett. 2009, 50, 3675 - 3678
    • (2009) Tetrahedron Lett. , vol.50 , pp. 3675-3678
    • Nambu, H.1    Hikime, M.2    Krishnamurthi, J.3    Kamiya, M.4    Shimada, N.5    Hashimoto, S.6
  • 400
    • 82355160842 scopus 로고    scopus 로고
    • Catalytic Enantioselective Intermolecular Cycloaddition of Diazodiketoester-Derived Carbonyl Ylides with Indoles Using Chiral Dirhodium(II) Carboxylates
    • Shimada, N.; Oohara, T.; Krishnamurthi, J.; Nambu, H.; Hashimoto, S. Catalytic Enantioselective Intermolecular Cycloaddition of Diazodiketoester-Derived Carbonyl Ylides with Indoles Using Chiral Dirhodium(II) Carboxylates Org. Lett. 2011, 13, 6284 - 6287
    • (2011) Org. Lett. , vol.13 , pp. 6284-6287
    • Shimada, N.1    Oohara, T.2    Krishnamurthi, J.3    Nambu, H.4    Hashimoto, S.5
  • 401
    • 34547178927 scopus 로고    scopus 로고
    • Catalytic Enantioselective Tandem Carbonyl Ylide Formation/1,3-Dipolar Cycloaddition Reactions of α-Diazo Ketones with Aromatic Aldehydes using Dirhodium(II) Tetrakis[N-benzene-fused-phthaloyl-(S)-valinate]
    • Tsutsui, H.; Shimada, N.; Abe, T.; Anada, M.; Nakajima, M.; Nakamura, S.; Nambu, H.; Hashimoto, S. Catalytic Enantioselective Tandem Carbonyl Ylide Formation/1,3-Dipolar Cycloaddition Reactions of α-Diazo Ketones with Aromatic Aldehydes using Dirhodium(II) Tetrakis[N-benzene-fused-phthaloyl-(S)-valinate] Adv. Synth. Catal. 2007, 349, 521 - 526
    • (2007) Adv. Synth. Catal. , vol.349 , pp. 521-526
    • Tsutsui, H.1    Shimada, N.2    Abe, T.3    Anada, M.4    Nakajima, M.5    Nakamura, S.6    Nambu, H.7    Hashimoto, S.8
  • 402
    • 77951829381 scopus 로고    scopus 로고
    • Catalytic Asymmetric Construction of the Exo-7-Aryl-6,8-dioxabicyclo[3.2.1]octane Framework of Psoracorylifols B and C Using a Carbonyl Ylide Cycloaddition Strategy
    • Kurosaki, Y.; Shimada, N.; Anada, M.; Nambu, H.; Hashimoto, S. Catalytic Asymmetric Construction of the Exo-7-Aryl-6,8-dioxabicyclo[3.2.1]octane Framework of Psoracorylifols B and C Using a Carbonyl Ylide Cycloaddition Strategy Bull. Korean Chem. Soc. 2010, 31, 694 - 696
    • (2010) Bull. Korean Chem. Soc. , vol.31 , pp. 694-696
    • Kurosaki, Y.1    Shimada, N.2    Anada, M.3    Nambu, H.4    Hashimoto, S.5
  • 403
    • 18944380156 scopus 로고    scopus 로고
    • 1,3-Dipolar Cycloadditions of Carbonyl Ylides to Aldimines: A Three-Component Approach to syn-α-Hydroxy-β-amino Esters
    • Torssell, S.; Kienle, M.; Somfai, P. 1,3-Dipolar Cycloadditions of Carbonyl Ylides to Aldimines: A Three-Component Approach to syn-α-Hydroxy-β-amino Esters Angew. Chem., Int. Ed. 2005, 44, 3096 - 3099
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 3096-3099
    • Torssell, S.1    Kienle, M.2    Somfai, P.3
  • 404
    • 33845293766 scopus 로고    scopus 로고
    • 1,3-Dipolar Cycloadditions of Carbonyl Ylides to Aldimines: Scope, Limitations and Asymmetric Cycloadditions
    • Torssell, S.; Somfai, P. 1,3-Dipolar Cycloadditions of Carbonyl Ylides to Aldimines: Scope, Limitations and Asymmetric Cycloadditions Adv. Synth. Catal. 2006, 348, 2421 - 2430
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 2421-2430
    • Torssell, S.1    Somfai, P.2
  • 405
    • 0001271260 scopus 로고    scopus 로고
    • Stereocontrol in Rare Earth Metal Triflate-Catalyzed 1,3-Dipolar Cycloaddition Reaction of 2-Benzopyrylium-4-olate with Aldehydes
    • Suga, H.; Kakehi, A.; Ito, S.; Inoue, K.; Ishida, H.; Ibata, T. Stereocontrol in Rare Earth Metal Triflate-Catalyzed 1,3-Dipolar Cycloaddition Reaction of 2-Benzopyrylium-4-olate with Aldehydes Org. Lett. 2000, 2, 3145 - 3148
    • (2000) Org. Lett. , vol.2 , pp. 3145-3148
    • Suga, H.1    Kakehi, A.2    Ito, S.3    Inoue, K.4    Ishida, H.5    Ibata, T.6
  • 406
    • 0034928995 scopus 로고    scopus 로고
    • Stereocontrol in a Ytterbium Triflate-Catalyzed 1,3-Dipolar Cycloaddition Reaction of Carbonyl Ylide with N-Substituted Maleimides and Dimethyl Fumarate
    • Suga, H.; Kakehi, A.; Ito, S.; Inoue, K.; Ishida, H.; Ibata, T. Stereocontrol in a Ytterbium Triflate-Catalyzed 1,3-Dipolar Cycloaddition Reaction of Carbonyl Ylide with N-Substituted Maleimides and Dimethyl Fumarate Bull. Chem. Soc. Jpn. 2001, 74, 1115 - 1121
    • (2001) Bull. Chem. Soc. Jpn. , vol.74 , pp. 1115-1121
    • Suga, H.1    Kakehi, A.2    Ito, S.3    Inoue, K.4    Ishida, H.5    Ibata, T.6
  • 407
    • 0037132621 scopus 로고    scopus 로고
    • Highly Enantioselective 1,3-Dipolar Cycloaddition Reactions of 2-Benzopyrylium-4-olate Catalyzed by Chiral Lewis Acids
    • Suga, H.; Inoue, K.; Inoue, S.; Kakehi, A. Highly Enantioselective 1,3-Dipolar Cycloaddition Reactions of 2-Benzopyrylium-4-olate Catalyzed by Chiral Lewis Acids J. Am. Chem. Soc. 2002, 124, 14836 - 14837
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 14836-14837
    • Suga, H.1    Inoue, K.2    Inoue, S.3    Kakehi, A.4
  • 408
    • 11844286891 scopus 로고    scopus 로고
    • Chiral 2,6-Bis(oxazolinyl)pyridine-Rare Earth Metal Complexes as Catalysts for Highly Enantioselective 1,3-Dipolar Cycloaddition Reactions of 2-Benzopyrylium-4-olates
    • Suga, H.; Inoue, K.; Inoue, S.; Kakehi, A.; Shiro, M. Chiral 2,6-Bis(oxazolinyl)pyridine-Rare Earth Metal Complexes as Catalysts for Highly Enantioselective 1,3-Dipolar Cycloaddition Reactions of 2-Benzopyrylium-4-olates J. Org. Chem. 2005, 70, 47 - 56
    • (2005) J. Org. Chem. , vol.70 , pp. 47-56
    • Suga, H.1    Inoue, K.2    Inoue, S.3    Kakehi, A.4    Shiro, M.5
  • 409
    • 33746983985 scopus 로고    scopus 로고
    • Asymmetric Cycloaddition Reactions between 2-Benzopyrylium-4-olates and 3-(2-Alkenoyl)-2-oxazolidinones in the Presence of 2,6-Bis(oxazolinyl)pyridine-Lanthanoid Complexes
    • Suga, H.; Suzuki, T.; Inoue, K.; Kakehi, A. Asymmetric Cycloaddition Reactions between 2-Benzopyrylium-4-olates And 3-(2-Alkenoyl)-2-oxazolidinones in the Presence of 2,6-Bis(oxazolinyl)pyridine-Lanthanoid Complexes Tetrahedron 2006, 62, 9218 - 9225
    • (2006) Tetrahedron , vol.62 , pp. 9218-9225
    • Suga, H.1    Suzuki, T.2    Inoue, K.3    Kakehi, A.4
  • 410
    • 84887089203 scopus 로고    scopus 로고
    • Chiral Lewis Acid Catalyzed Asymmetric Cycloadditions of Carbonyl Ylides Generated from Diazoimide Derivatives and their Synthetic Applications to Indolizidine Alkaloids
    • Suga, H.; Hashimoto, Y.; Yasumura, S.; Takezawa, R.; Itoh, K.; Kakehi, A. Chiral Lewis Acid Catalyzed Asymmetric Cycloadditions of Carbonyl Ylides Generated from Diazoimide Derivatives and their Synthetic Applications to Indolizidine Alkaloids J. Org. Chem. 2013, 78, 10840 - 10852
    • (2013) J. Org. Chem. , vol.78 , pp. 10840-10852
    • Suga, H.1    Hashimoto, Y.2    Yasumura, S.3    Takezawa, R.4    Itoh, K.5    Kakehi, A.6
  • 411
    • 35548978110 scopus 로고    scopus 로고
    • Dipole-LUMO/Dipolarophile-HOMO Controlled Asymmetric Cycloadditions of Carbonyl Ylides Catalyzed by Chiral Lewis Acids
    • Suga, H.; Ishimoto, D.; Higuchi, S.; Ohtsuka, M.; Arikawa, T.; Tsuchida, T.; Kakehi, A.; Baba, T. Dipole-LUMO/Dipolarophile-HOMO Controlled Asymmetric Cycloadditions of Carbonyl Ylides Catalyzed by Chiral Lewis Acids Org. Lett. 2007, 9, 4359 - 4362
    • (2007) Org. Lett. , vol.9 , pp. 4359-4362
    • Suga, H.1    Ishimoto, D.2    Higuchi, S.3    Ohtsuka, M.4    Arikawa, T.5    Tsuchida, T.6    Kakehi, A.7    Baba, T.8
  • 412
    • 77949567244 scopus 로고    scopus 로고
    • Inverse Electron Demand Asymmetric Cycloadditions of Cyclic Carbonyl Ylides Catalyzed by Chiral Lewis Acids-Scope and Limitations of Diazo and Olefinic Substrates
    • Suga, H.; Higuchi, S.; Ohtsuka, M.; Ishimoto, D.; Arikawa, T.; Hashimoto, Y.; Misawa, S.; Tsuchida, T.; Kakehi, A.; Baba, T. Inverse Electron Demand Asymmetric Cycloadditions of Cyclic Carbonyl Ylides Catalyzed by Chiral Lewis Acids-Scope and Limitations of Diazo and Olefinic Substrates Tetrahedron 2010, 66, 3070 - 3089
    • (2010) Tetrahedron , vol.66 , pp. 3070-3089
    • Suga, H.1    Higuchi, S.2    Ohtsuka, M.3    Ishimoto, D.4    Arikawa, T.5    Hashimoto, Y.6    Misawa, S.7    Tsuchida, T.8    Kakehi, A.9    Baba, T.10
  • 413
    • 84893488912 scopus 로고    scopus 로고
    • Catalytic Asymmetric [3 + 2] Cycloaddition of Aromatic Aldehydes with Oxiranes by C-C Bond Cleavage of Epoxides: Highly Efficient Synthesis of Chiral 1,3-Dioxolanes
    • Chen, W.; Lin, L.; Cai, Y.; Xia, Y.; Cao, W.; Liu, X.; Feng, X. Catalytic Asymmetric [3 + 2] Cycloaddition of Aromatic Aldehydes with Oxiranes by C-C Bond Cleavage of Epoxides: Highly Efficient Synthesis of Chiral 1,3-Dioxolanes Chem. Commun. 2014, 50, 2161 - 2163
    • (2014) Chem. Commun. , vol.50 , pp. 2161-2163
    • Chen, W.1    Lin, L.2    Cai, Y.3    Xia, Y.4    Cao, W.5    Liu, X.6    Feng, X.7
  • 414
    • 5444269981 scopus 로고
    • Ethyl Diazoacetate
    • Searle, N. E. Ethyl Diazoacetate Org. Synth. 1956, 36, 25 - 27
    • (1956) Org. Synth. , vol.36 , pp. 25-27
    • Searle, N.E.1
  • 415
    • 84981809697 scopus 로고
    • New Methods of Preparative Organic Chemistry. Transfer of Diazo Groups
    • Regitz, M. New Methods of Preparative Organic Chemistry. Transfer of Diazo Groups Angew. Chem., Int. Ed. Engl. 1967, 6, 733 - 749
    • (1967) Angew. Chem., Int. Ed. Engl. , vol.6 , pp. 733-749
    • Regitz, M.1
  • 416
    • 13044308051 scopus 로고
    • Synthese von α-Diazo-carbonylverbindungen durch Entformylierende Diazogruppenübertragung
    • Regitz, M.; Menz, F.; Rüter, J. Synthese von α-Diazo-carbonylverbindungen durch Entformylierende Diazogruppenübertragung Tetrahedron Lett. 1967, 8, 739 - 742
    • (1967) Tetrahedron Lett. , vol.8 , pp. 739-742
    • Regitz, M.1    Menz, F.2    Rüter, J.3
  • 417
    • 85065251590 scopus 로고
    • An Improved Preparation of α-Diazocarbonyl Compounds
    • Ledon, H. An Improved Preparation of α-Diazocarbonyl Compounds Synthesis 1974, 347 - 348
    • (1974) Synthesis , pp. 347-348
    • Ledon, H.1
  • 418
    • 0345986943 scopus 로고
    • Diazo Transfer by Means of Phase-Transfer Catalysis: Di- tert -butyl Diazomalonate
    • Ledon, H. J. Diazo Transfer by Means of Phase-Transfer Catalysis: Di- tert -butyl Diazomalonate Org. Synth. 1979, 59, 66 - 69
    • (1979) Org. Synth. , vol.59 , pp. 66-69
    • Ledon, H.J.1
  • 420
    • 0042197943 scopus 로고
    • Einwirkung von Diazoessigäther auf die Aether ungesättigter Säuren
    • Buchner, E. Einwirkung von Diazoessigäther auf die Aether ungesättigter Säuren Ber. Dtsch. Chem. Ges. 1888, 21, 2637 - 2647
    • (1888) Ber. Dtsch. Chem. Ges. , vol.21 , pp. 2637-2647
    • Buchner, E.1
  • 422
    • 0034327703 scopus 로고    scopus 로고
    • Lewis Acid-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions of Diazoalkane: Chiral Ligand/Achiral Auxiliary Cooperative Chirality Control
    • Kanemasa, S.; Kanai, T. Lewis Acid-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions of Diazoalkane: Chiral Ligand/Achiral Auxiliary Cooperative Chirality Control J. Am. Chem. Soc. 2000, 122, 10710 - 10711
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 10710-10711
    • Kanemasa, S.1    Kanai, T.2
  • 423
    • 33644542082 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloaddition Reaction between Diazoacetates and α-Substituted Acroleins: Total Synthesis of Manzacidin A
    • Kano, T.; Hashimoto, T.; Maruoka, K. Enantioselective 1,3-Dipolar Cycloaddition Reaction between Diazoacetates and α-Substituted Acroleins: Total Synthesis of Manzacidin A J. Am. Chem. Soc. 2006, 128, 2174 - 2175
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 2174-2175
    • Kano, T.1    Hashimoto, T.2    Maruoka, K.3
  • 424
    • 43249091655 scopus 로고    scopus 로고
    • Syntheses of Manzacidins: A Stage for the Demonstration of Synthetic Methodologies
    • Hashimoto, T.; Maruoka, K. Syntheses of Manzacidins: A Stage for the Demonstration of Synthetic Methodologies Org. Biomol. Chem. 2008, 6, 829 - 835
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 829-835
    • Hashimoto, T.1    Maruoka, K.2
  • 425
    • 84888857768 scopus 로고    scopus 로고
    • Development of Synthetic Transformations by Control of Acid-Catalyzed Reactions of Diazocarbonyl Compounds
    • Hashimoto, T.; Maruoka, K. Development of Synthetic Transformations by Control of Acid-Catalyzed Reactions of Diazocarbonyl Compounds Bull. Chem. Soc. Jpn. 2013, 86, 1217 - 1230
    • (2013) Bull. Chem. Soc. Jpn. , vol.86 , pp. 1217-1230
    • Hashimoto, T.1    Maruoka, K.2
  • 426
    • 69949181507 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Alkyl Diazoacetates with α,β-Disubstituted Acroleins
    • Gao, L.; Hwang, G. S.; Lee, M. Y.; Ryu, D. H. Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Alkyl Diazoacetates with α,β-Disubstituted Acroleins Chem. Commun. 2009, 5460 - 5462
    • (2009) Chem. Commun. , pp. 5460-5462
    • Gao, L.1    Hwang, G.S.2    Lee, M.Y.3    Ryu, D.H.4
  • 427
    • 34247474844 scopus 로고    scopus 로고
    • Enantioselective 1,3-Dipolar Cycloadditions of Diazoacetates with Electron-Deficient Olefins
    • Sibi, M. P.; Stanley, L. M.; Soeta, T. Enantioselective 1,3-Dipolar Cycloadditions of Diazoacetates with Electron-Deficient Olefins Org. Lett. 2007, 9, 1553 - 1556
    • (2007) Org. Lett. , vol.9 , pp. 1553-1556
    • Sibi, M.P.1    Stanley, L.M.2    Soeta, T.3
  • 428
    • 80052733253 scopus 로고    scopus 로고
    • Asymmetric Cycloaddition Reactions of Diazoesters with 2-Alkenoic Acid Derivatives Catalyzed by Binaphthyldiimine-Ni(II) Complexes
    • Suga, H.; Furihata, Y.; Sakamoto, A.; Itoh, K.; Okumura, Y.; Tsuchida, T.; Kakehi, A.; Baba, T. Asymmetric Cycloaddition Reactions of Diazoesters with 2-Alkenoic Acid Derivatives Catalyzed by Binaphthyldiimine-Ni(II) Complexes J. Org. Chem. 2011, 76, 7377 - 7387
    • (2011) J. Org. Chem. , vol.76 , pp. 7377-7387
    • Suga, H.1    Furihata, Y.2    Sakamoto, A.3    Itoh, K.4    Okumura, Y.5    Tsuchida, T.6    Kakehi, A.7    Baba, T.8
  • 429
    • 0037099395 scopus 로고    scopus 로고
    • A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective "ligation" of Azides and Terminal Alkynes
    • Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective "Ligation" of Azides and Terminal Alkynes Angew. Chem., Int. Ed. 2002, 41, 2596 - 2599
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 430
    • 0037012920 scopus 로고    scopus 로고
    • Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
    • Tornoe, C. W.; Christensen, C.; Meldal, M. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides J. Org. Chem. 2002, 67, 3057 - 3064
    • (2002) J. Org. Chem. , vol.67 , pp. 3057-3064
    • Tornoe, C.W.1    Christensen, C.2    Meldal, M.3
  • 431
  • 432
    • 84912571352 scopus 로고    scopus 로고
    • Enantioposition-Selective Copper-Catalyzed Azide-Alkyne Cycloaddition for Construction of Chiral Biaryl Derivatives
    • Osako, T.; Uozumi, Y. Enantioposition-Selective Copper-Catalyzed Azide-Alkyne Cycloaddition for Construction of Chiral Biaryl Derivatives Org. Lett. 2014, 16, 5866 - 5869
    • (2014) Org. Lett. , vol.16 , pp. 5866-5869
    • Osako, T.1    Uozumi, Y.2
  • 433
    • 35948953157 scopus 로고    scopus 로고
    • Distortion/Interaction Energy Control of 1,3-Dipolar Cycloaddition Reactivity
    • Ess, D. H.; Houk, K. N. Distortion/Interaction Energy Control of 1,3-Dipolar Cycloaddition Reactivity J. Am. Chem. Soc. 2007, 129, 10646 - 10647
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 10646-10647
    • Ess, D.H.1    Houk, K.N.2


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