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Volumn 21, Issue 6, 2009, Pages 619-627

Asymmetric Henry reaction catalyzed by bifunctional copper-based catalysts

Author keywords

Amino alcohol; Asymmetric reaction; Bifunctional catalyst; Henry reaction; Salen ligands

Indexed keywords

1 (2 HYDROXYBENZYLIDENEAMINO) 2,3 DIHYDRO 1H INDEN 2 OL; 1 (3,5 DI TERT BUTYL 2 HYDROXYBENZYLIDENEAMINO) 2,3 DIHYDRO 1H INDEN 2 OL; 2 (2 METHOXYBENZYLIDENEAMINO) 1,2 DIPHENYLETHANOL; 2 [(1 PHENYLETHYLIMINO)METHYL]PHENOL; 2 [(2 HYDROXY 1,2 DIPHENYLETHYLIMINO)METHYL] 4,6 DI TERT BUTYLPHENOL; 2 [(2 HYDROXY 1,2 DIPHENYLETHYLIMINO)METHYL]NAPHTHALEN 2 OL; 2 [(2 HYDROXY 1,2 DIPHENYLETHYLIMINO)METHYL]PHENOL; ALCOHOL; ALDEHYDE; CHEMICAL COMPOUND; COPPER; NITROGEN; NITROMETHANE; UNCLASSIFIED DRUG;

EID: 68349097408     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20661     Document Type: Article
Times cited : (32)

References (59)
  • 1
    • 0000851805 scopus 로고    scopus 로고
    • Uncatalyzed additions of nucleophilic alkenes to C=X
    • Trost BM, Fleming I, Heathcock CH, editors. New York: Pergamon;
    • Rosini G. Uncatalyzed additions of nucleophilic alkenes to C=X. Comprehensive organic synthesis. In: Trost BM, Fleming I, Heathcock CH, editors. New York: Pergamon; 1996. vol. 2, p 321.
    • (1996) Comprehensive organic synthesis , vol.2 , pp. 321
    • Rosini, G.1
  • 2
    • 0035804426 scopus 로고    scopus 로고
    • The Henry reaction: Recent examples
    • Luzio FA. The Henry reaction: recent examples. Tetrahedron 2001;57: 915-945.
    • (2001) Tetrahedron , vol.57 , pp. 915-945
    • Luzio, F.A.1
  • 4
    • 34250620600 scopus 로고    scopus 로고
    • Recent advances in the catalytic asymmetric nitroaldol (Henry) reaction
    • Palomo C, Oiarbide M, Laso A. Recent advances in the catalytic asymmetric nitroaldol (Henry) reaction. Eur J Org Chem 2007;16:2561-2574.
    • (2007) Eur J Org Chem , vol.16 , pp. 2561-2574
    • Palomo, C.1    Oiarbide, M.2    Laso, A.3
  • 7
    • 26244449129 scopus 로고    scopus 로고
    • A total synthesis of (-)-bestatin using Shibasaki's asymmetric Henry reaction
    • Gogoi N, Boruwa J, Barua NC. A total synthesis of (-)-bestatin using Shibasaki's asymmetric Henry reaction. Tetrahedron Lett 2005;46: 7581-7582.
    • (2005) Tetrahedron Lett , vol.46 , pp. 7581-7582
    • Gogoi, N.1    Boruwa, J.2    Barua, N.C.3
  • 8
    • 17444403980 scopus 로고    scopus 로고
    • Highly efficient approach to orthogonally protected (2S,4R)- and (2S,4S)-4-hydroxyornithine
    • Paintner FF, Allmendinger L, Bauschke G, Klemann P. Highly efficient approach to orthogonally protected (2S,4R)- and (2S,4S)-4-hydroxyornithine. Org Lett 2005;7:1423-1426.
    • (2005) Org Lett , vol.7 , pp. 1423-1426
    • Paintner, F.F.1    Allmendinger, L.2    Bauschke, G.3    Klemann, P.4
  • 9
    • 3843138591 scopus 로고    scopus 로고
    • Stereoselective synthesis of constrained oxacyclic hydroxyethylene isosteres of aspartyl protease inhibitors. Nitroaldol methodology toward 2,3-substituted tetrahydrofurans
    • Hanessian S, Brassard M, Stereoselective synthesis of constrained oxacyclic hydroxyethylene isosteres of aspartyl protease inhibitors. Nitroaldol methodology toward 2,3-substituted tetrahydrofurans. Tetrahedron 2004;60:7621-7628.
    • (2004) Tetrahedron , vol.60 , pp. 7621-7628
    • Hanessian, S.1    Brassard, M.2
  • 10
    • 1842686290 scopus 로고    scopus 로고
    • A highly efficient synthesis of the C-13 side-chain of taxol using Shibasaki's asymmetric Henry reaction
    • Borah JC, Gogoi S, Boruwa J, Kalita B, Barua NC. A highly efficient synthesis of the C-13 side-chain of taxol using Shibasaki's asymmetric Henry reaction. Tetrahedron Lett 2004;45:3689-3691.
    • (2004) Tetrahedron Lett , vol.45 , pp. 3689-3691
    • Borah, J.C.1    Gogoi, S.2    Boruwa, J.3    Kalita, B.4    Barua, N.C.5
  • 11
    • 84945959007 scopus 로고
    • Basic character of rare earth metal alkoxides. Utilization in catalytic carbon-carbon bond-forming reactions and catalytic asymmetric nitroaldol reactions
    • Sasai H, Suzuki T, Arai S, Shibasaki M. Basic character of rare earth metal alkoxides. Utilization in catalytic carbon-carbon bond-forming reactions and catalytic asymmetric nitroaldol reactions. J Am Chem Soc 1992;114:4418-4420.
    • (1992) J Am Chem Soc , vol.114 , pp. 4418-4420
    • Sasai, H.1    Suzuki, T.2    Arai, S.3    Shibasaki, M.4
  • 12
    • 27544433063 scopus 로고    scopus 로고
    • Guanidine-thiourea bifunctional organocatalyst for the asymmetric Henry (nitroaldol) reaction
    • Sohtome Y, Hashimoto Y, Nagasawa K. Guanidine-thiourea bifunctional organocatalyst for the asymmetric Henry (nitroaldol) reaction. Adv Synth Catal 2005;347:1643-1648.
    • (2005) Adv Synth Catal , vol.347 , pp. 1643-1648
    • Sohtome, Y.1    Hashimoto, Y.2    Nagasawa, K.3
  • 13
    • 33745825158 scopus 로고    scopus 로고
    • Diastereoselective and enantioselective Henry (nitroaldol) reaction utilizing a guanidine-thiourea bifunctional organocatalyst
    • Sohtome Y, Hashimoto Y, Nagasawa K. Diastereoselective and enantioselective Henry (nitroaldol) reaction utilizing a guanidine-thiourea bifunctional organocatalyst. Eur J Org Chem 2006;2894-2897.
    • (2006) Eur J Org Chem , pp. 2894-2897
    • Sohtome, Y.1    Hashimoto, Y.2    Nagasawa, K.3
  • 15
    • 31444439419 scopus 로고    scopus 로고
    • Enantioselective nitroaldol reaction of α-ketoesters catalyzed by cinchona alkaloids
    • Li H, Wang B, Deng L. Enantioselective nitroaldol reaction of α-ketoesters catalyzed by cinchona alkaloids. J Am Chem Soc 2006;128:732-733.
    • (2006) J Am Chem Soc , vol.128 , pp. 732-733
    • Li, H.1    Wang, B.2    Deng, L.3
  • 16
    • 0037466989 scopus 로고    scopus 로고
    • Designer chiral quaternary ammonium bifluorides as an efficient catalyst for asymmetric nitroaldol reaction of silyl nitronates with aromatic aldehydes
    • Ooi T, Doda K, Maruoka K. Designer chiral quaternary ammonium bifluorides as an efficient catalyst for asymmetric nitroaldol reaction of silyl nitronates with aromatic aldehydes. J Am Chem Soc 2003;125:2054-2055.
    • (2003) J Am Chem Soc , vol.125 , pp. 2054-2055
    • Ooi, T.1    Doda, K.2    Maruoka, K.3
  • 17
    • 0033549552 scopus 로고    scopus 로고
    • re- and si-Face-selective nitroaldol reactions catalyzed by a rigid chiral quaternary ammonium salt: A highly stereo-selective synthesis of the HIV protease inhibitor amprenavir (Vertex 478)
    • Corey EJ, Zhang FY. re- and si-Face-selective nitroaldol reactions catalyzed by a rigid chiral quaternary ammonium salt: a highly stereo-selective synthesis of the HIV protease inhibitor amprenavir (Vertex 478). Angew Chem Int Ed Engl 1999;38:1931-1934.
    • (1999) Angew Chem Int Ed Engl , vol.38 , pp. 1931-1934
    • Corey, E.J.1    Zhang, F.Y.2
  • 18
    • 35349001124 scopus 로고    scopus 로고
    • Chiral tetraaminophosphonium salt-mediated asymmetric direct Henry reaction
    • Uraguchi D, Sakaki S, Ooi T. Chiral tetraaminophosphonium salt-mediated asymmetric direct Henry reaction. J Am Chem Soc 2007;129:12392-12393.
    • (2007) J Am Chem Soc , vol.129 , pp. 12392-12393
    • Uraguchi, D.1    Sakaki, S.2    Ooi, T.3
  • 20
    • 36649026949 scopus 로고    scopus 로고
    • Development of axially chiral bis(arylthiourea)-based organocatalysts and their application in the enantioselective Henry reaction
    • Liu XG, Jiang JJ, Shi M. Development of axially chiral bis(arylthiourea)-based organocatalysts and their application in the enantioselective Henry reaction. Tetrahedron: Asymmetry 2007;18:2773-2781.
    • (2007) Tetrahedron: Asymmetry , vol.18 , pp. 2773-2781
    • Liu, X.G.1    Jiang, J.J.2    Shi, M.3
  • 21
    • 34249894998 scopus 로고    scopus 로고
    • Synthesis of novel chiral Schiff-base ligands and their application in asymmetric nitro aldol (Henry) reaction
    • Çolak M, Aral T, Hoşgören H, Demirel N. Synthesis of novel chiral Schiff-base ligands and their application in asymmetric nitro aldol (Henry) reaction. Tetrahedron: Asymmetry 2007;18:1129-1133.
    • (2007) Tetrahedron: Asymmetry , vol.18 , pp. 1129-1133
    • Çolak, M.1    Aral, T.2    Hoşgören, H.3    Demirel, N.4
  • 22
    • 34447109358 scopus 로고    scopus 로고
    • Development of new chiral phosphine-salen type ligands and their application in the Cu(I)-catalyzed enantioselective Henry reaction
    • Jiang JJ, Shi M. Development of new chiral phosphine-salen type ligands and their application in the Cu(I)-catalyzed enantioselective Henry reaction. Tetrahedron: Asymmetry 2007;18:1376-1382.
    • (2007) Tetrahedron: Asymmetry , vol.18 , pp. 1376-1382
    • Jiang, J.J.1    Shi, M.2
  • 23
    • 40849094003 scopus 로고    scopus 로고
    • Enantioselective nitroaldol (Henry) reaction catalyzed by chiral Schiff-base ligands
    • Çolak M, Aral T, Demirel N. Enantioselective nitroaldol (Henry) reaction catalyzed by chiral Schiff-base ligands. Tetrahedron: Asymmetry 2008;19:635-639.
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 635-639
    • Çolak, M.1    Aral, T.2    Demirel, N.3
  • 24
    • 34249002709 scopus 로고    scopus 로고
    • Novel thiolated amino-alcohols as chiral ligands for copper-catalyzed asymmetric nitro-aldol reactions
    • Mansawat W, Saengswang I, U-prasitwong P, Bhanthumnavin W, Vilaivan T. Novel thiolated amino-alcohols as chiral ligands for copper-catalyzed asymmetric nitro-aldol reactions. Tetrahedron Lett 2007; 48:4235-4238.
    • (2007) Tetrahedron Lett , vol.48 , pp. 4235-4238
    • Mansawat, W.1    Saengswang, I.2    U-prasitwong, P.3    Bhanthumnavin, W.4    Vilaivan, T.5
  • 25
    • 36148983364 scopus 로고    scopus 로고
    • Asymmetric nitroaldol reaction catalyzed by a chromium(III)-salen system
    • Kowalczyk R, Sidorowicz Ł, Skar_zewski J. Asymmetric nitroaldol reaction catalyzed by a chromium(III)-salen system. Tetrahedron: Asymmetry 2007;18:2581-2586.
    • (2007) Tetrahedron: Asymmetry , vol.18 , pp. 2581-2586
    • Kowalczyk, R.1    Sidorowicz, Ł.2    Skar-zewski, J.3
  • 26
    • 33846457382 scopus 로고    scopus 로고
    • A New copper(I)-tetrahydrosalen-catalyzed asymmetric Henry reaction and its extension to the synthesis of (S)-norphenylephrine
    • Xiong Y, Wang F, Huang X, Wen YH, Feng XM. A New copper(I)-tetrahydrosalen-catalyzed asymmetric Henry reaction and its extension to the synthesis of (S)-norphenylephrine. Chem Eur J 2007;13:829-833.
    • (2007) Chem Eur J , vol.13 , pp. 829-833
    • Xiong, Y.1    Wang, F.2    Huang, X.3    Wen, Y.H.4    Feng, X.M.5
  • 28
    • 34547150066 scopus 로고    scopus 로고
    • Enantioselective Henry reaction catalyzed with copper(II)-iminopyridine complexes
    • Blay G, Climent E, Fernández-Olmos V, Pedro JR. Enantioselective Henry reaction catalyzed with copper(II)-iminopyridine complexes. Tetrahedron: Asymmetry 2007;18:1603-1612.
    • (2007) Tetrahedron: Asymmetry , vol.18 , pp. 1603-1612
    • Blay, G.1    Climent, E.2    Fernández-Olmos, V.3    Pedro, J.R.4
  • 29
    • 46649103106 scopus 로고    scopus 로고
    • A library of chiral imidazoline-aminophenol ligands: Discovery of an efficient reaction sphere
    • Arai T, Yokoyama N, Yanagisawa A. A library of chiral imidazoline-aminophenol ligands: discovery of an efficient reaction sphere. Chem Eur J 2008;14:2052-2059.
    • (2008) Chem Eur J , vol.14 , pp. 2052-2059
    • Arai, T.1    Yokoyama, N.2    Yanagisawa, A.3
  • 30
    • 34250666228 scopus 로고    scopus 로고
    • Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation
    • Bandini M, Benaglia M, Sinisi R, Tommasi S, Umani-Ronchi A. Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation. Org Lett 2007;9:2151-2153.
    • (2007) Org Lett , vol.9 , pp. 2151-2153
    • Bandini, M.1    Benaglia, M.2    Sinisi, R.3    Tommasi, S.4    Umani-Ronchi, A.5
  • 31
    • 33645791471 scopus 로고    scopus 로고
    • Efficient and enantioselective nitroaldol reaction catalyzed by copper schiff-base complexes
    • Gan CS, Lai GY, Zhang ZH, Wang ZY, Zhou MM. Efficient and enantioselective nitroaldol reaction catalyzed by copper schiff-base complexes. Tetrahedron: Asymmetry 2006;17:725-728.
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 725-728
    • Gan, C.S.1    Lai, G.Y.2    Zhang, Z.H.3    Wang, Z.Y.4    Zhou, M.M.5
  • 32
    • 0142040727 scopus 로고    scopus 로고
    • A new copper acetate-bis(oxazoline)-catalyzed, enantioselective Henry reaction
    • Evans DA, Seidel D, Rueping M, Lam HW, Shaw JT, Downey CW. A new copper acetate-bis(oxazoline)-catalyzed, enantioselective Henry reaction. J Am Chem Soc 2003;125:12692-12693.
    • (2003) J Am Chem Soc , vol.125 , pp. 12692-12693
    • Evans, D.A.1    Seidel, D.2    Rueping, M.3    Lam, H.W.4    Shaw, J.T.5    Downey, C.W.6
  • 33
    • 0037725799 scopus 로고    scopus 로고
    • Catalytic asymmetric Henry reactions of silyl nitronates with aldehydes
    • Risgaard T, Gothelf KV, Jørgensen KA. Catalytic asymmetric Henry reactions of silyl nitronates with aldehydes. Org Biomol Chem 2003;1:153-156.
    • (2003) Org Biomol Chem , vol.1 , pp. 153-156
    • Risgaard, T.1    Gothelf, K.V.2    Jørgensen, K.A.3
  • 34
    • 7444242815 scopus 로고    scopus 로고
    • 2-symmetric tridentate bis(thiazoline) and bis(oxazoline) ligands and their application in the enantioselective Henry reaction
    • 2-symmetric tridentate bis(thiazoline) and bis(oxazoline) ligands and their application in the enantioselective Henry reaction. Tetrahedron: Asymmetry 2004;15:3433-3441.
    • (2004) Tetrahedron: Asymmetry , vol.15 , pp. 3433-3441
    • Lu, S.F.1    Du, D.M.2    Zhang, S.W.3    Xu, J.X.4
  • 35
  • 36
    • 17744381382 scopus 로고    scopus 로고
    • 2-symmetric tridentate bis(oxazoline) and bis(thiazoline) complexes: Metal-controlled reversal of enantioselectivity
    • 2-symmetric tridentate bis(oxazoline) and bis(thiazoline) complexes: metal-controlled reversal of enantioselectivity. J Org Chem 2005;70:3712-3715.
    • (2005) J Org Chem , vol.70 , pp. 3712-3715
    • Du, D.M.1    Lu, S.F.2    Fang, T.3    Xu, J.X.4
  • 37
  • 38
    • 34250632623 scopus 로고    scopus 로고
    • Rational design of sterically and electronically easily tunable chiral bisimidazolines and their applications in dual lewis acid/ brosted base catalysis for highly enantioselective nitroaldol (Henry) reactions
    • Ma KY, You JS. Rational design of sterically and electronically easily tunable chiral bisimidazolines and their applications in dual lewis acid/ brosted base catalysis for highly enantioselective nitroaldol (Henry) reactions. Chem Eur J 2007;13:1863-1871.
    • (2007) Chem Eur J , vol.13 , pp. 1863-1871
    • Ma, K.Y.1    You, J.S.2
  • 40
    • 0036495323 scopus 로고    scopus 로고
    • A dinuclear zn catalyst for the asymmetric nitroaldol (Henry) reaction
    • Trost BM, Yeh VSC. A dinuclear zn catalyst for the asymmetric nitroaldol (Henry) reaction. Angew Chem Int Ed Engl 2002;41:861-863.
    • (2002) Angew Chem Int Ed Engl , vol.41 , pp. 861-863
    • Trost, B.M.1    Yeh, V.S.C.2
  • 41
    • 0037043532 scopus 로고    scopus 로고
    • Effect of ligand structure on the zinc-catalyzed Henry reaction asymmetric syntheses of (-)-Denopamine and (-)-Arbutamine
    • Trost BM, Yeh VSC, Ito H, Bremeyer N. Effect of ligand structure on the zinc-catalyzed Henry reaction asymmetric syntheses of (-)-Denopamine and (-)-Arbutamine. Org Lett 2002;4:2621-2623.
    • (2002) Org Lett , vol.4 , pp. 2621-2623
    • Trost, B.M.1    Yeh, V.S.C.2    Ito, H.3    Bremeyer, N.4
  • 42
    • 1442277240 scopus 로고    scopus 로고
    • Zhong TU, Tian P, Lin GQ. New β-amino alcohols with a bicyclo[3.3.0] octane scaffold in an asymmetric Henry reaction. Tetrahedron: Asymmetry 2004;15:771-776.
    • Zhong TU, Tian P, Lin GQ. New β-amino alcohols with a bicyclo[3.3.0] octane scaffold in an asymmetric Henry reaction. Tetrahedron: Asymmetry 2004;15:771-776.
  • 43
    • 21244472399 scopus 로고    scopus 로고
    • Enantioselective Henry reactions under dual lewis acid/amine catalysis using chiral amino alcohol ligands
    • Palomo C, Oiarbide M, Laso A. Enantioselective Henry reactions under dual lewis acid/amine catalysis using chiral amino alcohol ligands. Angew Chem Int Ed Engl 2005;44:3881-3884.
    • (2005) Angew Chem Int Ed Engl , vol.44 , pp. 3881-3884
    • Palomo, C.1    Oiarbide, M.2    Laso, A.3
  • 44
    • 3242786409 scopus 로고    scopus 로고
    • Enantioselective Henry reaction catalyzed by optically active ketoiminatocobalt complexes
    • Kogami Y, Nakajima T, Ashizawa T, Kezuka S, Ikeno T, Yamada T. Enantioselective Henry reaction catalyzed by optically active ketoiminatocobalt complexes. Chem Lett 2004;614-615.
    • (2004) Chem Lett , pp. 614-615
    • Kogami, Y.1    Nakajima, T.2    Ashizawa, T.3    Kezuka, S.4    Ikeno, T.5    Yamada, T.6
  • 45
    • 4444257618 scopus 로고    scopus 로고
    • Enantioselective Henry reaction catalyzed by salen-cobalt complexes
    • Kogami Y, Nakajima T, Ikeno T, Yamada T. Enantioselective Henry reaction catalyzed by salen-cobalt complexes. Synthesis 2004;12:1947-1950.
    • (2004) Synthesis , vol.12 , pp. 1947-1950
    • Kogami, Y.1    Nakajima, T.2    Ikeno, T.3    Yamada, T.4
  • 46
    • 0034987398 scopus 로고    scopus 로고
    • Multifunctional asymmetric catalysis
    • Shibasaki M, Kanai M. Multifunctional asymmetric catalysis. Chem Pharm Bull 2001;49:511-524.
    • (2001) Chem Pharm Bull , vol.49 , pp. 511-524
    • Shibasaki, M.1    Kanai, M.2
  • 47
    • 0035905571 scopus 로고    scopus 로고
    • The development of new monometallic bifunctional catalysts with lewis acid and lewis base properties, and their application in asymmetric cyanation reactions
    • Gröger H. The development of new monometallic bifunctional catalysts with lewis acid and lewis base properties, and their application in asymmetric cyanation reactions. Chem Eur J 2001;7:5246-5251.
    • (2001) Chem Eur J , vol.7 , pp. 5246-5251
    • Gröger, H.1
  • 48
    • 0036402658 scopus 로고    scopus 로고
    • Recent progress in asymmetric two-center catalysis
    • Shibasaki M, Kanai M, Funabashi K. Recent progress in asymmetric two-center catalysis. Chem Commun 2002;1989-1999.
    • (2002) Chem Commun , pp. 1989-1999
    • Shibasaki, M.1    Kanai, M.2    Funabashi, K.3
  • 49
    • 0037087605 scopus 로고    scopus 로고
    • Aluminum-catalyzed asymmetric addition of TMSCN to aromatic and aliphatic ketones promoted by an easily accessible and recyclable peptide ligand
    • Deng H, Isler MP, Snapper ML, Hoveyda AH. Aluminum-catalyzed asymmetric addition of TMSCN to aromatic and aliphatic ketones promoted by an easily accessible and recyclable peptide ligand. Angew Chem Int Ed Engl 2002;41:1009-1012.
    • (2002) Angew Chem Int Ed Engl , vol.41 , pp. 1009-1012
    • Deng, H.1    Isler, M.P.2    Snapper, M.L.3    Hoveyda, A.H.4
  • 50
    • 0034596326 scopus 로고    scopus 로고
    • Catalytic enantioselective cyanosilylation of ketones
    • Hamashima Y, Kanai M, Shibasaki M. Catalytic enantioselective cyanosilylation of ketones. J Am Chem Soc 2000;122:7412-7413.
    • (2000) J Am Chem Soc , vol.122 , pp. 7412-7413
    • Hamashima, Y.1    Kanai, M.2    Shibasaki, M.3
  • 51
    • 0013130960 scopus 로고    scopus 로고
    • The first catalytic asymmetric addition of dialkylzincs to a-ketoesters
    • DiMauro E, Kozlowski M. The first catalytic asymmetric addition of dialkylzincs to a-ketoesters. Org Lett 2002;4:3781-3784.
    • (2002) Org Lett , vol.4 , pp. 3781-3784
    • DiMauro, E.1    Kozlowski, M.2
  • 52
    • 0030600186 scopus 로고    scopus 로고
    • 2Zn to aldehydes promoted by a chiral Schiff base metal complex
    • 2Zn to aldehydes promoted by a chiral Schiff base metal complex. Tetrahedron Lett 1996;37:4613-4615.
    • (1996) Tetrahedron Lett , vol.37 , pp. 4613-4615
    • Cozzi, P.G.1    Papa, A.2    Umani-Ronchi, A.3
  • 53
    • 0038711344 scopus 로고    scopus 로고
    • Enantioselective alkynylation of ketones catalyzed by Zn(salen) complexes
    • Cozzi PG. Enantioselective alkynylation of ketones catalyzed by Zn(salen) complexes. Angew Chem Int Ed Engl 2003;42:2895-2898.
    • (2003) Angew Chem Int Ed Engl , vol.42 , pp. 2895-2898
    • Cozzi, P.G.1
  • 54
    • 0035799157 scopus 로고    scopus 로고
    • Ambifunctional cooperative catalysts
    • Rowlands GJ. Ambifunctional cooperative catalysts. Tedrahedron 2001;57:1865-1882.
    • (2001) Tedrahedron , vol.57 , pp. 1865-1882
    • Rowlands, G.J.1
  • 56
    • 41149115644 scopus 로고    scopus 로고
    • Highly enantioselective alkynylation of aldehydes catalyzed by a new oxazolidine-titanium complex
    • Xu Z, Mao JC, Zhang YW. Highly enantioselective alkynylation of aldehydes catalyzed by a new oxazolidine-titanium complex. Org Biomol Chem 2008;6:1288-1292.
    • (2008) Org Biomol Chem , vol.6 , pp. 1288-1292
    • Xu, Z.1    Mao, J.C.2    Zhang, Y.W.3
  • 57
    • 10844234849 scopus 로고    scopus 로고
    • Concise synthesis of novel practical sulfamide-amine alcohols for the enantioselective addition of diethylzinc to aldehydes
    • Mao JC, Wan BS, Wang RL, Wu F, Lu SW. Concise synthesis of novel practical sulfamide-amine alcohols for the enantioselective addition of diethylzinc to aldehydes. J Org Chem 2004;69:9123-9127.
    • (2004) J Org Chem , vol.69 , pp. 9123-9127
    • Mao, J.C.1    Wan, B.S.2    Wang, R.L.3    Wu, F.4    Lu, S.W.5
  • 58
    • 0037181367 scopus 로고    scopus 로고
    • Ruck RT, Jacobsen EN. Asymmetric catalysis of hetero-ene reactions with tridentate schiff base chromium(III) complexes. J Am Chem Soc 2002;124:2882-2883.
    • Ruck RT, Jacobsen EN. Asymmetric catalysis of hetero-ene reactions with tridentate schiff base chromium(III) complexes. J Am Chem Soc 2002;124:2882-2883.
  • 59
    • 8644289262 scopus 로고    scopus 로고
    • Highly enantioselective cyanosilylation of aldehydes catalyzed by novel β-amino alcohol-titanium complexes
    • Li Y, Qin B, Feng X. Highly enantioselective cyanosilylation of aldehydes catalyzed by novel β-amino alcohol-titanium complexes. J Org Chem 2004;69:7910-7913.
    • (2004) J Org Chem , vol.69 , pp. 7910-7913
    • Li, Y.1    Qin, B.2    Feng, X.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.