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Volumn 18, Issue 9, 2014, Pages 1073-1096

Organocatalysis in synthesis of pyrrolidine derivatives via cycloaddition reactions of azomethine ylides

Author keywords

Azomethine ylides; Cycloadditions; Organocatalysis; Pyrrolidines; Stereoselectivity

Indexed keywords

CATALYSIS; HYDROCARBONS; ORGANOCATALYST; RATE CONSTANTS; STEREOSELECTIVITY; SULFURIC ACID; SYNTHESIS (CHEMICAL);

EID: 84904036369     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/1385272819999140404130229     Document Type: Article
Times cited : (30)

References (116)
  • 1
    • 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
  • 2
    • 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
  • 3
    • 33745819966 scopus 로고    scopus 로고
    • Conjugated azomethine ylides
    • Pinho e Melo, T.M.V.D. Conjugated azomethine ylides. Eur. J. Org. Chem., 2006, 2006, 2873-2888.
    • (2006) Eur. J. Org. Chem , vol.2006 , pp. 2873-2888
    • Pinho1    Melo, T.M.V.D.2
  • 4
    • 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
  • 5
    • 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
  • 6
    • 70450181011 scopus 로고    scopus 로고
    • Microwave-assisted 1,3-dipolar cycloaddition: An eco-friendly approach to five-membered heterocycles
    • Pineiro, M.; Pinho e Melo, T.M.V.D. Microwave-assisted 1,3-dipolar cycloaddition: an eco-friendly approach to five-membered heterocycles. Eur. J. Org. Chem., 2009, 2009, 5287-5307.
    • (2009) Eur. J. Org. Chem , vol.2009 , pp. 5287-5307
    • Pineiro, M.1    Pinho e Melo, T.M.V.D.2
  • 7
    • 79959795429 scopus 로고    scopus 로고
    • Novel dipolarophiles and dipoles in the metalcatalyzed enantioselective 1,3-dipolar cycloaddition of azomethine ylides
    • Adrio, J.; Carretero, J.C. Novel dipolarophiles and dipoles in the metalcatalyzed 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
  • 8
    • 8744290197 scopus 로고
    • Alan R. Katritzky, Ed.; Academic Press: San Diego
    • Tsuge, O.; Kanemasa, S. In: Advances in Heterocyclic Chemistry; Alan R. Katritzky, Ed.; Academic Press: San Diego, 1989; Vol. 45, pp. 231-349.
    • (1989) Advances In Heterocyclic Chemistry , vol.45 , pp. 231-349
    • Tsuge, O.1    Kanemasa, S.2
  • 9
    • 84869001482 scopus 로고    scopus 로고
    • Kinetic study of thermal 1,3-dipolar cycloaddition of azomethine ylides by using differential scanning calorimetry
    • Mancebo-Aracil, J.; Muñoz-Guillena, M.J.; Such-Basáñez, I.; Sansano-Gil, J.M. Kinetic study of thermal 1,3-dipolar cycloaddition of azomethine ylides by using differential scanning calorimetry. ChemPlusChem, 2012, 77, 770-777.
    • (2012) ChemPlusChem , vol.77 , pp. 770-777
    • Mancebo-Aracil, J.1    Muñoz-Guillena, M.J.2    Such-Basáñez, I.3    Sansano-Gil, J.M.4
  • 11
    • 0000789414 scopus 로고
    • X=Y-ZH systems as potential 1,3-dipoles. Part 26. 1,5-electrocyclisation and tandem 1,5-electrocyclisation. Aldol type condensation processes in imines
    • Grigg, R.; Nimal Gunaratne, H.Q.; Henderson, D.; Sridharan, V. X=Y-ZH systems as potential 1,3-dipoles. Part 26. 1,5-electrocyclisation and tandem 1,5-electrocyclisation. Aldol type condensation processes in imines. Tetrahedron, 1990, 46, 1599-1610.
    • (1990) Tetrahedron , vol.46 , pp. 1599-1610
    • Grigg, R.1    Nimal, G.H.Q.2    Henderson, D.3    Sridharan, V.4
  • 12
    • 0028841963 scopus 로고
    • X=Y-ZH systems as potential 1,3-dipoles. Part 46.1 cascade 1,3-dipolar cycloaddition reactions of cephalosporin imines
    • Grigg, R.; McMeekin, P.; Sridharan, V. X=Y-ZH systems as potential 1,3-dipoles. Part 46.1 cascade 1,3-dipolar cycloaddition reactions of cephalosporin imines. Tetrahedron, 1995, 51, 13347-13356.
    • (1995) Tetrahedron , vol.51 , pp. 13347-13356
    • Grigg, R.1    McMeekin, P.2    Sridharan, V.3
  • 13
    • 79955750733 scopus 로고    scopus 로고
    • An exoand enantioselective 1,3-dipolar cycloaddition of azomethine ylides with alkylidene malonates catalyzed by a N,O-ligand/Cu(OAc)2-derived chiral complex
    • Wang, M.; Wang, Z.; Shi, Y.H.; Shi, X.X.; Fossey, J.S.; Deng, W.P. An exoand enantioselective 1,3-dipolar cycloaddition of azomethine ylides with alkylidene malonates catalyzed by a N,O-ligand/Cu(OAc)2-derived chiral complex. Angew. Chem. Int. Ed., 2011, 50, 4897-4900.
    • (2011) Angew. Chem. Int. Ed , vol.50 , pp. 4897-4900
    • Wang, M.1    Wang, Z.2    Shi, Y.H.3    Shi, X.X.4    Fossey, J.S.5    Deng, W.P.6
  • 14
    • 84867901560 scopus 로고    scopus 로고
    • Asymmetric [3+2] cycloaddition of azomethine ylides catalyzed by silver(I) triflate with a chiral bipyrrolidinederived phosphine ligand
    • Gu, X.; Xu, Z.J.; Lo, V.; Che, C.M. Asymmetric [3+2] cycloaddition of azomethine ylides catalyzed by silver(I) triflate with a chiral bipyrrolidinederived phosphine ligand. Synthesis, 2012, 44, 3307-3314.
    • (2012) Synthesis , vol.44 , pp. 3307-3314
    • Gu, X.1    Xu, Z.J.2    Lo, V.3    Che, C.M.4
  • 15
    • 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
  • 16
    • 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
  • 17
    • 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 Cózar, 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 Cózar, A.4    Cossío, F.P.5
  • 19
    • 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
  • 20
    • 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
  • 21
    • 84861965132 scopus 로고    scopus 로고
    • Cu(I)/DTBM-BIPHEP-catalyzed exo-selective 1,3-dipolar cycloaddition of azomethine ylides with cistrifluorocrotonate 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 cistrifluorocrotonate 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
  • 22
    • 84883452412 scopus 로고    scopus 로고
    • Cu-mediated 1,3-dipolar cycloaddition of azomethine ylides with dipolarophiles: A faster access to spirooxindoles of potential pharmacological interest
    • Singh, S.N.; Regati, S.; Paul, A.K.; Layek, M.; Jayaprakash, S.; Reddy, K.V.; Deora, G.S.; Mukherjee, S.; Pal, M. Cu-mediated 1,3-dipolar cycloaddition of azomethine ylides with dipolarophiles: a faster access to spirooxindoles of potential pharmacological interest. Tetrahedron Lett., 2013, 54, 5448-5452.
    • (2013) Tetrahedron Lett , vol.54 , pp. 5448-5452
    • Singh, S.N.1    Regati, S.2    Paul, A.K.3    Layek, M.4    Jayaprakash, S.5    Reddy, K.V.6    Deora, G.S.7    Mukherjee, S.8    Pal, M.9
  • 23
    • 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
  • 24
    • 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
  • 25
    • 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
  • 26
    • 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-Asymm., 2012, 23, 306-312.
    • (2012) Tetrahedron-Asymm , vol.23 , pp. 306-312
    • Han, M.L.1    Wang, D.Y.2    Zeng, P.W.3    Zheng, Z.4    Hu, X.P.5
  • 27
    • 84879325650 scopus 로고    scopus 로고
    • Phosphoramidite-Cu(OTf)2 complexes as chiral catalysts for 1,3-dipolar cycloaddition of iminoesters and nitroalkenes
    • Castelló, L.M.; Nájera, C.; Sansano, J.M.; Larrañaga, O.; Cózar, A. de; Cossío, F.P. Phosphoramidite-Cu(OTf)2 complexes as chiral catalysts for 1,3-dipolar cycloaddition of iminoesters and nitroalkenes. Org. Lett., 2013, 15, 2902-2905.
    • (2013) Org. Lett , vol.15 , pp. 2902-2905
    • Castelló, L.M.1    Nájera, C.2    Sansano, J.M.3    Larrañaga, O.4    de Cózar, A.5    Cossío, F.P.6
  • 28
    • 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
  • 29
    • 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
  • 30
    • 0003497902 scopus 로고    scopus 로고
    • Kobayashi, S.; Jørgensen, K.A., Eds.; Wiley-VCH Verlag GmbH: Weinheim, FRG
    • Gothelf, K.V. In: Cycloaddition Reactions in Organic Synthesis; Kobayashi, S.; Jørgensen, K.A., Eds.; Wiley-VCH Verlag GmbH: Weinheim, FRG, 2002; pp. 211-247.
    • (2002) Cycloaddition Reactions In Organic Synthesis , pp. 211-247
    • Gothelf, K.V.1
  • 31
    • 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
  • 32
    • 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-Asymm., 2005, 16, 2047-2061.
    • (2005) Tetrahedron-Asymm , vol.16 , pp. 2047-2061
    • Husinec, S.1    Savic, V.2
  • 33
    • 84871997136 scopus 로고    scopus 로고
    • Applications of asymmetric organocatalysis in medicinal chemistry
    • Alemán, J.; Cabrera, S. Applications of asymmetric organocatalysis in medicinal chemistry. Chem. Soc. Rev., 2013, 42, 774-793.
    • (2013) Chem. Soc. Rev , vol.42 , pp. 774-793
    • Alemán, J.1    Cabrera, S.2
  • 34
    • 84879543822 scopus 로고    scopus 로고
    • Asymmetric organocatalysis mediated by -ldiaryl prolinols: Recent advances
    • Meninno, S.; Lattanzi, A. Asymmetric organocatalysis mediated by -ldiaryl prolinols: recent advances. Chem. Commun., 2013, 49, 3821-3832.
    • (2013) Hem. Commun , vol.9 , pp. 821-3832
    • Meninno, S.1    Lattanzi, A.2
  • 35
    • 84886163782 scopus 로고    scopus 로고
    • Dunn, P.J.; Hii, K.K.M.; Krische, M.J.; Williams, M.T., Eds.; John Wiley & Sons, Inc.: Hoboken, New Jersey
    • Gotoh, H.; Hayashi, Y. In: Sustainable Catalysis; Dunn, P.J.; Hii, K.K.M.; Krische, M.J.; Williams, M.T., Eds.; John Wiley & Sons, Inc.: Hoboken, New Jersey, 2013; pp. 287-316.
    • (2013) Sustainable Catalysis , pp. 287-316
    • Gotoh, H.1    Hayashi, Y.2
  • 36
    • 84874733534 scopus 로고    scopus 로고
    • Guanidine organocatalysis
    • Selig, P. Guanidine organocatalysis. Synthesis, 2013, 45, 703-718.
    • (2013) Synthesis , vol.45 , pp. 703-718
    • Selig, P.1
  • 38
    • 84874403013 scopus 로고    scopus 로고
    • Soluble polymer-supported organocatalysts
    • Yang, Y.C.; Bergbreiter, D.E. Soluble polymer-supported organocatalysts. Pure Appl. Chem., 2013, 85, 493-509.
    • (2013) Pure Appl. Chem , vol.85 , pp. 493-509
    • Yang, Y.C.1    Bergbreiter, D.E.2
  • 39
    • 84885617025 scopus 로고    scopus 로고
    • Recent advances in organocatalytic methods for asymmetric C-C bond formation
    • Scheffler, U.; Mahrwald, R. Recent advances in organocatalytic methods for asymmetric C-C bond formation. Chem-Eur. J., 2013, 19, 14346-14396.
    • (2013) Chem-Eur. J , vol.19 , pp. 14346-14396
    • Scheffler, U.1    Mahrwald, R.2
  • 40
    • 47749122232 scopus 로고    scopus 로고
    • Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, FRG
    • Berkessel, A.; Gröger, H. In: Asymmetric Organocatalysis; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, FRG, 2005; pp. 256-268.
    • (2005) Asymmetric Organocatalysis , pp. 256-268
    • Berkessel, A.1    Gröger, H.2
  • 41
    • 84861508079 scopus 로고    scopus 로고
    • Dalko, P.I., Ed.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, FRG
    • Dalko, P.I. In: Enantioselective Organocatalysis; Dalko, P.I., Ed.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, FRG, 2007; pp. 1-17.
    • (2007) Enantioselective Organocatalysis , pp. 1-17
    • Dalko, P.I.1
  • 42
    • 52149113820 scopus 로고    scopus 로고
    • The advent and development of organocatalysis
    • MacMillan, D.W.C. The advent and development of organocatalysis. Nature, 2008, 455, 304-308.
    • (2008) Nature , vol.455 , pp. 304-308
    • Macmillan, D.W.C.1
  • 43
    • 37549005156 scopus 로고    scopus 로고
    • Organocatalysis lost: Modern chemistry, ancient chemistry, and an unseen biosynthetic apparatus
    • Barbas, C.F. Organocatalysis lost: Modern chemistry, ancient chemistry, and an unseen biosynthetic apparatus. Angew. Chem. Int. Ed., 2008, 47, 42-47.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 42-47
    • Barbas, C.F.1
  • 45
    • 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
  • 46
    • 80051716582 scopus 로고    scopus 로고
    • Asymmetric organocatalytic cyclization and cycloaddition reactions
    • Moyano, A.; Rios, R. Asymmetric organocatalytic cyclization and cycloaddition reactions. Chem. Rev., 2011, 111, 4703-4832.
    • (2011) Chem. Rev , vol.111 , pp. 4703-4832
    • Moyano, A.1    Rios, R.2
  • 47
    • 84887100406 scopus 로고    scopus 로고
    • List-Barbas-Mannich reaction catalyzed by modularly designed organocatalysts
    • Perera, S.; Sinha, D.; Rana, N.K.; Trieu-Do, V.; Zhao, J.C.G. List-Barbas-Mannich reaction catalyzed by modularly designed organocatalysts. J. Org. Chem., 2013, 78, 10947-10953.
    • (2013) J. Org. Chem , vol.78 , pp. 10947-10953
    • Perera, S.1    Sinha, D.2    Rana, N.K.3    Trieu-Do, V.4    Zhao, J.C.G.5
  • 48
    • 79955813687 scopus 로고    scopus 로고
    • N-Prolinylanthranilic acid derivatives as bifunctional organocatalysts for asymmetric aldol reactions
    • Pearson, A.J.; Panda, S. N-Prolinylanthranilic acid derivatives as bifunctional organocatalysts for asymmetric aldol reactions. Tetrahedron, 2011, 67, 3969-3975.
    • (2011) Tetrahedron , vol.67 , pp. 3969-3975
    • Pearson, A.J.1    Panda, S.2
  • 49
    • 77957929482 scopus 로고    scopus 로고
    • Organocatalytic asymmetric tandem Michael addition-hemiacetalization: A route to chiral dihydrocoumarins, chromanes, and 4 H-chromenes
    • Lu, D.; Li, Y.; Gong, Y. Organocatalytic asymmetric tandem Michael addition-hemiacetalization: A route to chiral dihydrocoumarins, chromanes, and 4 H-chromenes. J. Org. Chem., 2010, 75, 6900-6907.
    • (2010) J. Org. Chem , vol.75 , pp. 6900-6907
    • Lu, D.1    Li, Y.2    Gong, Y.3
  • 50
    • 84869054562 scopus 로고    scopus 로고
    • Organocatalytic Michael addition of nitro esters to α,β-unsaturated aldehydes: Towards the enantioselective synthesis of trans-3-substituted proline derivatives
    • Han, M.Y.; Zhang, Y.; Wang, H.Z.; An, W.K.; Ma, B.C.; Zhang, Y.; Wang, W. Organocatalytic Michael addition of nitro esters to α,β-unsaturated aldehydes: Towards the enantioselective synthesis of trans-3-substituted proline derivatives. Adv. Synth. Catal., 2012, 354, 2635-2640.
    • (2012) Adv. Synth. Catal , vol.354 , pp. 2635-2640
    • Han, M.Y.1    Zhang, Y.2    Wang, H.Z.3    An, W.K.4    Ma, B.C.5    Zhang, Y.6    Wang, W.7
  • 51
    • 84876732609 scopus 로고    scopus 로고
    • Unique properties of chiral biaryl-based secondary amine catalysts for asymmetric enamine catalysis
    • Kano, T.; Maruoka, K. Unique properties of chiral biaryl-based secondary amine catalysts for asymmetric enamine catalysis. Chem. Sci., 2013, 4, 907-915.
    • (2013) Chem. Sci , vol.4 , pp. 907-915
    • Kano, T.1    Maruoka, K.2
  • 54
    • 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
  • 55
    • 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
  • 56
    • 84883490378 scopus 로고    scopus 로고
    • The organocatalytic enantioselective [3+2] cycloaddition reaction of α,β-unsaturated aldehydes with azomethine ylides applied to the asymmetric synthesis of densely substituted pyrroloisoquinolines
    • Iza, A.; Ugarriza, I.; Uria, U.; Reyes, E.; Carrillo, L.; Vicario, J.L. The organocatalytic enantioselective [3+2] cycloaddition reaction of α,β-unsaturated aldehydes with azomethine ylides applied to the asymmetric synthesis of densely substituted pyrroloisoquinolines. Tetrahedron, 2013, 69, 8878-8884.
    • (2013) Tetrahedron , vol.69 , pp. 8878-8884
    • Iza, A.1    Ugarriza, I.2    Uria, U.3    Reyes, E.4    Carrillo, L.5    Vicario, J.L.6
  • 57
    • 77951133319 scopus 로고    scopus 로고
    • The organocatalytic [3+2] cycloaddition of azomethine ylides and α,β--unsaturated aldehydes as a convenient tool for the enantioselective synthesis of pyrrolizidines and indolizidines
    • Iza, A.; Carrillo, L.; Vicario, J.L.; Badía, D.; Reyes, E.; Martínez, J.I. The organocatalytic [3+2] cycloaddition of azomethine ylides and α,β--unsaturated aldehydes as a convenient tool for the enantioselective synthesis of pyrrolizidines and indolizidines. Org. Biomol. Chem., 2010, 8, 2238-2244.
    • (2010) Org. Biomol. Chem , vol.8 , pp. 2238-2244
    • Iza, A.1    Carrillo, L.2    Vicario, J.L.3    Badía, D.4    Reyes, E.5    Martínez, J.I.6
  • 58
    • 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
  • 59
    • 84255162188 scopus 로고    scopus 로고
    • Complete 2,5-diastereocontrol in the organocatalytic enantioselective [3+2] cycloaddition of enals with azomethine ylides derived from β-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 β-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
  • 60
    • 79961241357 scopus 로고    scopus 로고
    • Dynamic one-Pot threecomponent 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 threecomponent 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
  • 61
    • 0347004674 scopus 로고    scopus 로고
    • 1,3-dipolar cycloaddition reactions of pyridinium azomethine ylides containing 5,6-dicyanopyrazines
    • Jaung, J.Y.; Jung, Y.S. 1,3-dipolar cycloaddition reactions of pyridinium azomethine ylides containing 5,6-dicyanopyrazines. B. Kor. Chem. Soc., 2003, 24, 1565-1566.
    • (2003) B. Kor. Chem. Soc , vol.24 , pp. 1565-1566
    • Jaung, J.Y.1    Jung, Y.S.2
  • 62
    • 23744482006 scopus 로고    scopus 로고
    • A novel one-pot, three-component access to hexahydropyrrolo[2,1-a]isoquinolines by an alkylation-dehydrohalogenation-1,3-dipolar cycloaddition sequence
    • Nyerges, M.; Somfai, B.; Tóth, J.; Téke, L.; Dancsó, A.; Blaskó, G. A novel one-pot, three-component access to hexahydropyrrolo[2,1-a]isoquinolines by an alkylation-dehydrohalogenation-1,3-dipolar cycloaddition sequence. Synthesis, 2005, 2005, 2039-2045.
    • (2005) Synthesis , vol.2005 , pp. 2039-2045
    • Nyerges, M.1    Somfai, B.2    Tóth, J.3    Téke, L.4    Dancsó, A.5    Blaskó, G.6
  • 63
    • 79955557380 scopus 로고    scopus 로고
    • Asymmetric synthesis of pyrrolo[2,1-a]isoquinoline derivatives by 1,3-dipolar cycloadditions of stabilized isoquinolinium N-ylides with sulfinyl dipolarophiles
    • García Ruano, J.L.; Fraile, A.; Martín, M.R.; González, G.; Fajardo, C.; Martín-Castro, A.M. Asymmetric synthesis of pyrrolo[2,1-a]isoquinoline derivatives by 1,3-dipolar cycloadditions of stabilized isoquinolinium N-ylides with sulfinyl dipolarophiles. J. Org. Chem., 2011, 76, 3296-3305.
    • (2011) J. Org. Chem , vol.76 , pp. 3296-3305
    • García, R.J.L.1    Fraile, A.2    Martín, M.R.3    González, G.4    Fajardo, C.5    Martín-Castro, A.M.6
  • 65
    • 0037170916 scopus 로고    scopus 로고
    • Kinetic acidity of iminium ions. 2-Alkynyl-and 2,5-dialkynyl-pyrrolidines via the iminium ion route to azomethine ylides
    • Grigg, R.; Sridharan, V.; Thornton-Pett, M.; Wang, J.; Xu, J.; Zhang, J. Kinetic acidity of iminium ions. 2-Alkynyl-and 2,5-dialkynyl-pyrrolidines via the iminium ion route to azomethine ylides. Tetrahedron, 2002, 58, 2627-2640.
    • (2002) Tetrahedron , vol.58 , pp. 2627-2640
    • Grigg, R.1    Sridharan, V.2    Thornton-Pett, M.3    Wang, J.4    Xu, J.5    Zhang, J.6
  • 66
    • 84876532805 scopus 로고    scopus 로고
    • Metal-free a-amination of secondary amines: Computational and experimental evidence for azaquinone methide and azomethine ylide intermediates
    • Dieckmann, A.; Richers, M.T.; Platonova, A.Y.; Zhang, C.; Seidel, D.; Houk, K.N. Metal-free a-amination of secondary amines: Computational and experimental evidence for azaquinone methide and azomethine ylide intermediates. J. Org. Chem., 2013, 78, 4132-4144.
    • (2013) J. Org. Chem , vol.78 , pp. 4132-4144
    • Dieckmann, A.1    Richers, M.T.2    Platonova, A.Y.3    Zhang, C.4    Seidel, D.5    Houk, K.N.6
  • 68
    • 84864129277 scopus 로고    scopus 로고
    • Reactions of pyridinium N-ylides and their related pyridinium salts
    • Kakehi, A. Reactions of pyridinium N-ylides and their related pyridinium salts. Heterocycles, 2012, 85, 1529-1577.
    • (2012) Heterocycles , vol.85 , pp. 1529-1577
    • Kakehi, A.1
  • 69
    • 77952394193 scopus 로고    scopus 로고
    • Regioselective synthesis of 3-acylindolizines and benzo-analogues via 1,3-dipolar cycloadditions of N-ylides with maleic anhydride
    • Liu, Y.; Zhang, Y.; Shen, Y.M.; Hu, H.W.; Xu, J.H. Regioselective synthesis of 3-acylindolizines and benzo-analogues via 1,3-dipolar cycloadditions of N-ylides with maleic anhydride. Org. Biomol. Chem., 2010, 8, 2449-2456.
    • (2010) Org. Biomol. Chem , vol.8 , pp. 2449-2456
    • Liu, Y.1    Zhang, Y.2    Shen, Y.M.3    Hu, H.W.4    Xu, J.H.5
  • 70
    • 0030825651 scopus 로고    scopus 로고
    • The first 1,7-electrocyclizations of butadienyl pyridinium ylides: Stereoselective formation of 1,2-annulated 2,3-dihydroazepines
    • Marx, K.; Eberbach, W. The first 1,7-electrocyclizations of butadienyl pyridinium ylides: Stereoselective formation of 1,2-annulated 2,3-dihydroazepines. Tetrahedron, 1997, 53, 14687-14700.
    • (1997) Tetrahedron , vol.53 , pp. 14687-14700
    • Marx, K.1    Eberbach, W.2
  • 71
    • 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
  • 72
    • 84857565386 scopus 로고    scopus 로고
    • Asymmetric synthesis of hexahydropyrrolo-isoquinolines by an organocatalytic three-component reaction
    • Fraile, A.; Scarpino Schietroma, D.M.; Albrecht, A.; Davis, R.L.; Jørgensen, K.A. Asymmetric synthesis of hexahydropyrrolo-isoquinolines by an organocatalytic three-component reaction. Chem-Eur. J., 2012, 18, 2773-2776.
    • (2012) Chem-Eur. J , vol.18 , pp. 2773-2776
    • Fraile, A.1    Scarpino Schietroma, D.M.2    Albrecht, A.3    Davis, R.L.4    Jørgensen, K.A.5
  • 73
    • 80053992962 scopus 로고    scopus 로고
    • Chiral Brønsted acids in enantioselective carbonyl activations-activation modes and applications
    • Rueping, M.; Kuenkel, A.; Atodiresei, I. Chiral Brønsted acids in enantioselective carbonyl activations-activation modes and applications. Chem. Soc. Rev., 2011, 40, 4539-4549.
    • (2011) Chem. Soc. Rev , vol.40 , pp. 4539-4549
    • Rueping, M.1    Kuenkel, A.2    Atodiresei, I.3
  • 74
    • 78149432679 scopus 로고    scopus 로고
    • Chiral BINOL-derived phosphoric acids: Privileged Brønsted acid organocatalysts for C-C bond formation reactions
    • Zamfir, A.; Schenker, S.; Freund, M.; Tsogoeva, S.B. Chiral BINOL-derived phosphoric acids: privileged Brønsted acid organocatalysts for C-C bond formation reactions. Org. Biomol. Chem., 2010, 8, 5262-5276.
    • (2010) Org. Biomol. Chem , vol.8 , pp. 5262-5276
    • Zamfir, A.1    Schenker, S.2    Freund, M.3    Tsogoeva, S.B.4
  • 75
    • 77953261329 scopus 로고    scopus 로고
    • Chiral phosphoric acids as versatile catalysts for enantioselective transformations
    • Terada, M. Chiral phosphoric acids as versatile catalysts for enantioselective transformations. Synthesis, 2010, 2010, 1929-1982.
    • (2010) Synthesis , vol.2010 , pp. 1929-1982
    • Terada, M.1
  • 76
    • 81255211335 scopus 로고    scopus 로고
    • Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles
    • Yu, J.; Shi, F.; Gong, L.Z. Brønsted-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
  • 77
    • 42649137921 scopus 로고    scopus 로고
    • Asymmetric organocatalytic threecomponent 1,3-dipolar cycloaddition: Control of stereochemistry via a chiral Brønsted acid activated dipole
    • Chen, X.H.; Zhang, W.Q.; Gong, L.Z. Asymmetric organocatalytic threecomponent 1,3-dipolar cycloaddition: Control of stereochemistry via a chiral Brønsted 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
  • 78
    • 70349742473 scopus 로고    scopus 로고
    • Organocatalytic synthesis of spiro[pyrrolidin-3,3 a -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 a -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
  • 79
    • 0004136903 scopus 로고
    • Curran, D.P., Ed.; JAI Press: Greenwich
    • Grigg, R.; Sridharan, V. In: Advances in Cycloaddition; Curran, D.P., Ed.; JAI Press: Greenwich, 1993; Vol. 3, pp. 161-204.
    • (1993) Advances In Cycloaddition , vol.3 , pp. 161-204
    • Grigg, R.1    Sridharan, V.2
  • 80
    • 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, 46, 1275-1277.
    • (2010) Chem. Commun , vol.46 , pp. 1275-1277
    • Wang, C.1    Chen, X.H.2    Zhou, S.M.3    Gong, L.Z.4
  • 81
    • 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
  • 82
    • 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
  • 83
    • 84875852473 scopus 로고    scopus 로고
    • Enantioselective construction of 2,5-dihydropyrrole skeleton with quaternary stereogenic center via catalytic asymmetric 1,3-dipolar cycloaddition involving a -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 a -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
  • 84
    • 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 a-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 a-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
  • 85
    • 61349181405 scopus 로고    scopus 로고
    • Direct assembly of aldehydes, amino esters, and anilines into chiral imidazolidines via Brønsted 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 Brønsted 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
  • 86
    • 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
  • 87
    • 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
  • 88
    • 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
  • 89
    • 84861544403 scopus 로고    scopus 로고
    • Scaffold-inspired enantioselective synthesis of biologically important spiro[pyrrolidin-3,2 a-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 a-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
  • 91
    • 0014961403 scopus 로고
    • The mechanism of transamination-function of the histidyl residue at the active site of supernatant aspartate transaminase
    • Peterson, D.L.; Martinez-Carrion, M. The mechanism of transamination-function of the histidyl residue at the active site of supernatant aspartate transaminase. J. Biol. Chem., 1970, 245, 806-813.
    • (1970) J. Biol. Chem , vol.245 , pp. 806-813
    • Peterson, D.L.1    Martinez-Carrion, M.2
  • 92
    • 0000127613 scopus 로고
    • Vitamin B6-catalyzed reactions of.alpha.-amino and.alpha.-keto acids: Model systems
    • Martell, A.E. Vitamin B6-catalyzed reactions of.alpha.-amino and.alpha.-keto acids: model systems. Acc. Chem. Res., 1989, 22, 115-124.
    • (1989) Acc. Chem. Res , vol.22 , pp. 115-124
    • Martell, A.E.1
  • 93
    • 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
  • 94
    • 84874943193 scopus 로고    scopus 로고
    • (±)-CSA catalyzed Friedel-Crafts alkylation of indoles with 3-ethoxycarbonyl-3-hydoxyisoindolin-1-one: An easy access of 3-ethoxycarbonyl-3-indolylisoindolin-1-ones bearing a quaternary a-amino acid moiety
    • Srivastava, A.; Singh, S.; Samanta, S. (±)-CSA catalyzed Friedel-Crafts alkylation of indoles with 3-ethoxycarbonyl-3-hydoxyisoindolin-1-one: an easy access of 3-ethoxycarbonyl-3-indolylisoindolin-1-ones bearing a quaternary a-amino acid moiety. Tetrahedron Lett., 2013, 54, 1444-1448.
    • (2013) Tetrahedron Lett , vol.54 , pp. 1444-1448
    • Srivastava, A.1    Singh, S.2    Samanta, S.3
  • 95
    • 79952745045 scopus 로고    scopus 로고
    • An efficient biomaterial supported bifunctional organocatalyst (ES-SO3-C5H5NH+) for the synthesis of a-amino carbonyls
    • Verma, S.; Jain, S.L.; Sain, B. An efficient biomaterial supported bifunctional organocatalyst (ES-SO3-C5H5NH+) for the synthesis of a-amino carbonyls. Org. Biomol. Chem., 2011, 9, 2314-2318.
    • (2011) Org. Biomol. Chem , vol.9 , pp. 2314-2318
    • Verma, S.1    Jain, S.L.2    Sain, B.3
  • 97
    • 84857355974 scopus 로고    scopus 로고
    • p-Sulfonic acid calix[n]arenes as homogeneous and recyclable organocatalysts for esterification reactions
    • Fernandes, S.A.; Natalino, R.; Gazolla, P.A.R.; da Silva, M.J.; Jham, G.N. p-Sulfonic acid calix[n]arenes as homogeneous and recyclable organocatalysts for esterification reactions. Tetrahedron Lett., 2012, 53, 1630-1633.
    • (2012) Tetrahedron Lett , vol.53 , pp. 1630-1633
    • Fernandes, S.A.1    Natalino, R.2    Gazolla, P.A.R.3    da Silva, M.J.4    Jham, G.N.5
  • 98
    • 80255138764 scopus 로고    scopus 로고
    • De p-Sulfonic acid calixarenes as efficient and reusable organocatalysts for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/-thiones
    • Da Silva, D.L.; Fernandes, S.A.; Sabino, A.A.; Fátima, Â. de p-Sulfonic acid calixarenes as efficient and reusable organocatalysts for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/-thiones. Tetrahedron Lett., 2011, 52, 6328-6330.
    • (2011) Tetrahedron Lett , vol.52 , pp. 6328-6330
    • da Silva, D.L.1    Fernandes, S.A.2    Sabino, A.A.3    Fátima, Â.4
  • 99
    • 77954555240 scopus 로고    scopus 로고
    • Diversity oriented synthesis of pyrrolidines via natural carbohydrate solid acid catalyst
    • Kumar, A.; Gupta, G.; Srivastava, S. Diversity oriented synthesis of pyrrolidines via natural carbohydrate solid acid catalyst. J. Comb. Chem., 2010, 12, 458-462.
    • (2010) J. Comb. Chem , vol.12 , pp. 458-462
    • Kumar, A.1    Gupta, G.2    Srivastava, S.3
  • 100
    • 63049095171 scopus 로고    scopus 로고
    • (Thio)urea organocatalysis-What can be learnt from anion recognition?
    • Zhang, Z.; Schreiner, P.R. (Thio)urea organocatalysis-What can be learnt from anion recognition? Chem. Soc. Rev., 2009, 38, 1187-1198.
    • (2009) Chem. Soc. Rev , vol.38 , pp. 1187-1198
    • Zhang, Z.1    Schreiner, P.R.2
  • 101
    • 44349168328 scopus 로고    scopus 로고
    • Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts
    • Connon, S.J. Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts. Chem. Commun., 2008, (22), 2499-2510.
    • (2008) Chem. Commun , Issue.22 , pp. 2499-2510
    • Connon, S.J.1
  • 102
    • 84885102458 scopus 로고    scopus 로고
    • Bifunctional primary aminethioureas in asymmetric organocatalysis
    • Serdyuk, O.V.; Heckel, C.M.; Tsogoeva, S.B. Bifunctional primary aminethioureas in asymmetric organocatalysis. Org. Biomol. Chem., 2013, 11, 7051-7071.
    • (2013) Org. Biomol. Chem , vol.11 , pp. 7051-7071
    • Serdyuk, O.V.1    Heckel, C.M.2    Tsogoeva, S.B.3
  • 103
    • 62249221359 scopus 로고    scopus 로고
    • The design of novel, synthetically useful (thio)urea-based organocatalysts
    • Connon, S. The design of novel, synthetically useful (thio)urea-based organocatalysts. Synlett, 2009, 2009, 354-376.
    • (2009) Synlett , vol.2009 , pp. 354-376
    • Connon, S.1
  • 104
    • 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, 2008, 691-694.
    • (2008) Synlett , vol.2008 , pp. 691-694
    • Xue, M.X.1    Zhang, X.M.2    Gong, L.Z.3
  • 105
    • 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
  • 106
    • 55449131123 scopus 로고    scopus 로고
    • Reaction control in the organocatalytic asymmetric one-pot, three-component reaction of aldehydes, diethyl-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-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
  • 107
    • 77951095904 scopus 로고    scopus 로고
    • Efficient kinetic resolution of racemic 3-nitro-2H-chromene derivatives catalyzed by Takemoto's organocatalyst
    • Xie, J.W.; Fan, L.P.; Su, H.; Li, X.S.; Xu, D.C. Efficient kinetic resolution of racemic 3-nitro-2H-chromene derivatives catalyzed by Takemoto's organocatalyst. Org. Biomol. Chem., 2010, 8, 2117-2122.
    • (2010) Org. Biomol. Chem , vol.8 , pp. 2117-2122
    • Xie, J.W.1    Fan, L.P.2    Su, H.3    Li, X.S.4    Xu, D.C.5
  • 108
    • 79961155855 scopus 로고    scopus 로고
    • Metal-free asymmetric 1,3-dipolar cycloaddition of Narylmaleimides 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 Narylmaleimides to azomethine ylides catalyzed by chiral tertiary amine thiourea. Eur. J. Org. Chem., 2011, 2011, 4472-4478.
    • (2011) Eur. J. Org. Chem , vol.2011 , 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
  • 109
    • 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
  • 110
    • 84555191597 scopus 로고    scopus 로고
    • Core structure-based design of organocatalytic [3+2]-cycloaddition reactions: Highly efficient and stereocontrolled syntheses of 3,3-pyrrolidonyl spirooxindoles
    • Tan, B.; Zeng, X.; Leong, W.W.Y.; Shi, Z.; Barbas, C.F.; Zhong, G. Core structure-based design of organocatalytic [3+2]-cycloaddition reactions: Highly efficient and stereocontrolled syntheses of 3,3-pyrrolidonyl spirooxindoles. Chem-Eur. J., 2012, 18, 63-67.
    • (2012) Chem-Eur. J , vol.18 , pp. 63-67
    • Tan, B.1    Zeng, X.2    Leong, W.W.Y.3    Shi, Z.4    Barbas, C.F.5    Zhong, G.6
  • 111
    • 84876530424 scopus 로고    scopus 로고
    • Efficient construction of highly functionalized spiro[-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[-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
  • 112
    • 79955624369 scopus 로고    scopus 로고
    • Ishikawa, T., Ed.; John Wiley & Sons, Ltd: Chichester, UK
    • Kumamoto, T. In: Superbases for Organic Synthesis; Ishikawa, T., Ed.; John Wiley & Sons, Ltd: Chichester, UK, 2009; pp. 295-313.
    • (2009) Superbases For Organic Synthesis , pp. 295-313
    • Kumamoto, T.1
  • 114
    • 0000805378 scopus 로고
    • Dugas, H.; Schmidtchen, F.P., Eds.; Springer Berlin Heidelberg: Berlin, Heidelberg
    • Hannon, C.L.; Anslyn, E.V. In: Bioorganic Chemistry Frontiers; Dugas, H.; Schmidtchen, F.P., Eds.; Springer Berlin Heidelberg: Berlin, Heidelberg, 1993; Vol. 3, pp. 193-255.
    • (1993) Bioorganic Chemistry Frontiers , vol.3 , pp. 193-255
    • Hannon, C.L.1    Anslyn, E.V.2
  • 115
    • 84889378743 scopus 로고    scopus 로고
    • Ishikawa, T., Ed.; John Wiley & Sons, Ltd: Chichester, UK
    • Nagasawa, K. In: Superbases for organic synthesis; Ishikawa, T., Ed.; John Wiley & Sons, Ltd: Chichester, UK, 2009; pp. 211-250.
    • (2009) Superbases For Organic Synthesis , pp. 211-250
    • Nagasawa, K.1
  • 116
    • 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, 2009, 1670-1674.
    • (2009) Synlett , vol.2009 , pp. 1670-1674
    • Nakano, M.1    Terada, M.2


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