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Volumn 15, Issue 13, 2011, Pages 2184-2209

Organocatalytic activation of imines and related compounds through hydrogen-bond interactions

Author keywords

Br nsted acids; Hydrogen bond; Imines; Organocatalysis; Phosphoric acids; Thioureas

Indexed keywords

CHEMICAL ACTIVATION; COMPLEXATION; HYDROGEN BONDS;

EID: 79959322101     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211796150660     Document Type: Review
Times cited : (8)

References (181)
  • 2
    • 85120582501 scopus 로고    scopus 로고
    • Enantioselective Organocatalysis, Ed
    • Enantioselective Organocatalysis; Dalko, P. I., Ed.; Wiley-VCH: Weinheim, 2007.
    • (2007) Wiley-VCH: Weinheim
    • Dalko, P.I.1
  • 3
    • 34250684250 scopus 로고    scopus 로고
    • Organocatalytic synthesis of drugs and bioactive natural products
    • and references cited therein
    • de Figuereido, R. M.; Christmann, M. Organocatalytic synthesis of drugs and bioactive natural products. Eur. J. Org. Chem. 2007, 2575-2600 and references cited therein.
    • (2007) Eur. J. Org. Chem. , pp. 2575-2600
    • de Figuereido, R.M.1    Christmann, M.2
  • 4
    • 33947570837 scopus 로고
    • The decomposition of β-nitrocarboxylic acids. With some remarks on the decomposition of β-ketocarboxylic acids
    • Pedersen, K. J. The decomposition of β-nitrocarboxylic acids. With some remarks on the decomposition of β-ketocarboxylic acids. J. Chem. Phys. 1934, 38, 559-571.
    • (1934) J. Chem. Phys. , vol.38 , pp. 559-571
    • Pedersen, K.J.1
  • 6
    • 84980123791 scopus 로고
    • Ueber eine Darstellungsweise der Glutarsäure
    • Knoevenagel, E. Ueber eine Darstellungsweise der Glutarsäure. Chem. Ber. 1894, 27, 2345-2346.
    • (1894) Chem. Ber. , vol.27 , pp. 2345-2346
    • Knoevenagel, E.1
  • 7
    • 84981750119 scopus 로고
    • Condensation von Malonsäure mit aromatischen Aldehyden durch Ammoniak und Amine
    • Knoevenagel, E. Condensation von Malonsäure mit aromatischen Aldehyden durch Ammoniak und Amine. Chem. Ber. 1898, 31, 2596-2619.
    • (1898) Chem. Ber. , vol.31 , pp. 2596-2619
    • Knoevenagel, E.1
  • 8
    • 0002788460 scopus 로고
    • Asymmetric synthesis caused by catalysts
    • Bredig, G.; Fiske, P. S. Asymmetric synthesis caused by catalysts. Biochem. Z. 1912, 46, 7-23.
    • (1912) Biochem. Z. , vol.46 , pp. 7-23
    • Bredig, G.1    Fiske, P.S.2
  • 9
    • 84981886574 scopus 로고
    • New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures
    • Eder, U.; Sauer, G.; Wiechert, R. New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures. Angew. Chem. Int. Ed. 1971, 10, 496-497.
    • (1971) Angew. Chem. Int. Ed. , vol.10 , pp. 496-497
    • Eder, U.1    Sauer, G.2    Wiechert, R.3
  • 10
    • 33847804003 scopus 로고
    • Asymmetric synthesis of bicyclic intermediates of natural product chemistry
    • Hajos, Z. G.; Parrish, D. R. Asymmetric synthesis of bicyclic intermediates of natural product chemistry. J. Org. Chem. 1974, 39, 1615-1621.
    • (1974) J. Org. Chem. , vol.39 , pp. 1615-1621
    • Hajos, Z.G.1    Parrish, D.R.2
  • 11
    • 15244343428 scopus 로고    scopus 로고
    • Asymmetric Organocatalysis
    • Seayad, J.; List, B. Asymmetric Organocatalysis. Org. Biomol. Chem. 2005, 3, 719-724.
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 719-724
    • Seayad, J.1    List, B.2
  • 12
    • 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
  • 13
    • 48849094479 scopus 로고    scopus 로고
    • Asymmetric Organocatalysis: From infancy to adolescence
    • Dondoni, A.; Massi, A. Asymmetric Organocatalysis: From infancy to adolescence. Angew. Chem. Int. Ed. 2008, 47, 4638-4660.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4638-4660
    • Dondoni, A.1    Massi, A.2
  • 14
    • 4143095871 scopus 로고    scopus 로고
    • Enamine catalysis is a powerful strategy for the catalytic generation and use of carbanion equivalents
    • List, B. Enamine catalysis is a powerful strategy for the catalytic generation and use of carbanion equivalents. Acc. Chem. Res. 2004, 37, 548-557.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 548-557
    • List, B.1
  • 17
    • 85196433245 scopus 로고    scopus 로고
    • In HOMO activation the energy of the highest-occupied molecular orbital (HOMO) is increased. In LUMO activation the energy of the lowestoccupied molecular orbital (LUMO) is decreased. In SOMO activation an electron is located in a singly occupied molecular orbital (SOMO) thus generating very reactive intermediates
    • In HOMO activation the energy of the highest-occupied molecular orbital (HOMO) is increased. In LUMO activation the energy of the lowestoccupied molecular orbital (LUMO) is decreased. In SOMO activation an electron is located in a singly occupied molecular orbital (SOMO) thus generating very reactive intermediates.
  • 18
    • 34250205588 scopus 로고    scopus 로고
    • Enantioselective organocatalytic singly occupied molecular orbital activation: The enantioselective enolation of aldehydes
    • Jang, H.-Y.; Hong, J.-B.; MacMillan, D. W. C. Enantioselective organocatalytic singly occupied molecular orbital activation: The enantioselective enolation of aldehydes. J. Am. Chem. Soc. 2007, 129, 7004-7005.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 7004-7005
    • Jang, H.-Y.1    Hong, J.-B.2    Macmillan, D.W.C.3
  • 19
    • 40149110106 scopus 로고    scopus 로고
    • Enantioselective organo-SOMO catalysis: The α- vinylation of aldehydes
    • Kim, H.; MacMillan, D. W. C. Enantioselective organo-SOMO catalysis: The α- vinylation of aldehydes. J. Am. Chem. Soc. 2008, 130, 398-399.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 398-399
    • Kim, H.1    Macmillan, D.W.C.2
  • 20
    • 57549095938 scopus 로고    scopus 로고
    • Enantioselective organo-singly occupied molecular orbital catalysis: The carbo-oxidation of styrenes
    • Graham, T. H.; Jones, C. M.; Jui, N. T.; MacMIllan, D. W. C. Enantioselective organo-singly occupied molecular orbital catalysis: The carbo-oxidation of styrenes. J. Am. Chem. Soc. 2008, 130, 16494-16495.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 16494-16495
    • Graham, T.H.1    Jones, C.M.2    Jui, N.T.3    Macmillan, D.W.C.4
  • 21
    • 69049104186 scopus 로고    scopus 로고
    • Enantioselective α-arylation of aldehydes via organo-SOMO catalysis. An ortho-selective arylation reaction based on an open-shell pathway
    • Conrad, J. C.; Kong, J.; Laforteza, B. N.; MacMillan, D. W. C. Enantioselective α-arylation of aldehydes via organo-SOMO catalysis. An ortho-selective arylation reaction based on an open-shell pathway. J. Am. Chem. Soc. 2009, 131, 11640-11641.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 11640-11641
    • Conrad, J.C.1    Kong, J.2    Laforteza, B.N.3    Macmillan, D.W.C.4
  • 22
    • 68849107137 scopus 로고    scopus 로고
    • Enantioselective aldehyde α-nitroalkylation via oxidative organocatalysis
    • Wilson, J. E.; Casarez, A. D.; MacMillan, D. W. C. Enantioselective aldehyde α-nitroalkylation via oxidative organocatalysis. J. Am. Chem. Soc. 2009, 131, 11332-11334.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 11332-11334
    • Wilson, J.E.1    Casarez, A.D.2    Macmillan, D.W.C.3
  • 23
    • 0041878745 scopus 로고    scopus 로고
    • Nucleophilic chiral amines as catalysts in asymmetric synthesis
    • France, S.; Guerin, D. J.; Miller, S. J.; Lectka, T. Nucleophilic chiral amines as catalysts in asymmetric synthesis. Chem. Rev. 2003, 103, 2985-3012.
    • (2003) Chem. Rev. , vol.103 , pp. 2985-3012
    • France, S.1    Guerin, D.J.2    Miller, S.J.3    Lectka, T.4
  • 24
    • 4143051292 scopus 로고    scopus 로고
    • Nucleophilic carbenes in asymmetric organocatalysis
    • Enders, D.; Balensiefer, T. Nucleophilic carbenes in asymmetric organocatalysis. Acc. Chem. Res. 2004, 37, 534-541.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 534-541
    • Enders, D.1    Balensiefer, T.2
  • 25
    • 38349109278 scopus 로고    scopus 로고
    • Organocatalysis by N-heterocyclic carbenes
    • Enders, D.; Niemeier, O.; Henseler, A. Organocatalysis by N-heterocyclic carbenes. Chem. Rev. 2007, 107, 5606-5655.
    • (2007) Chem. Rev. , vol.107 , pp. 5606-5655
    • Enders, D.1    Niemeier, O.2    Henseler, A.3
  • 26
    • 5144220014 scopus 로고    scopus 로고
    • Nucleophilic phosphine organocatalysis
    • Methot, J. L.; Roush, W. R. Nucleophilic phosphine organocatalysis. Adv. Synth. Catal. 2004, 346, 1035-1050.
    • (2004) Adv. Synth. Catal. , vol.346 , pp. 1035-1050
    • Methot, J.L.1    Roush, W.R.2
  • 28
    • 0346865819 scopus 로고    scopus 로고
    • Metal-free organocatalysis through explicit hydrogen bonding interactions
    • Schreiner, P. R. Metal-free organocatalysis through explicit hydrogen bonding interactions Chem. Soc. Rev. 2003, 32, 289-296.
    • (2003) Chem. Soc. Rev. , vol.32 , pp. 289-296
    • Schreiner, P.R.1
  • 29
    • 38349135345 scopus 로고    scopus 로고
    • Small-molecule H-bond donors in asymmetric catalysis
    • Doyle, A. G.; Jacobsen, E. N. Small-molecule H-bond donors in asymmetric catalysis. Chem. Rev. 2007, 107, 5713-5743.
    • (2007) Chem. Rev. , vol.107 , pp. 5713-5743
    • Doyle, A.G.1    Jacobsen, E.N.2
  • 30
    • 33646468489 scopus 로고    scopus 로고
    • Asymmetric catalysis by chiral hydrogen-bond donors
    • Taylor, M. S.; Jacobsen, E. N. Asymmetric catalysis by chiral hydrogen-bond donors. Angew. Chem. Int. Ed. 2006, 45, 1520-1543.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 1520-1543
    • Taylor, M.S.1    Jacobsen, E.N.2
  • 31
    • 44349168328 scopus 로고    scopus 로고
    • Asymmetric catalysis with bifunctional cinchona alkaloidbased urea and thiourea organocatalysts
    • Connon, S. J. Asymmetric catalysis with bifunctional cinchona alkaloidbased urea and thiourea organocatalysts. Chem. Commun. 2008, 2499-2510.
    • (2008) Chem. Commun. , pp. 2499-2510
    • Connon, S.J.1
  • 32
    • 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
  • 33
    • 53549091362 scopus 로고    scopus 로고
    • Discovery and application of asymmetric reaction by multi-functional thioureas
    • Miyabe, H.; Takemoto, Y. Discovery and application of asymmetric reaction by multi-functional thioureas. Bull. Chem. Soc. Jpn. 2008, 81, 785-795.
    • (2008) Bull. Chem. Soc. Jpn. , vol.81 , pp. 785-795
    • Miyabe, H.1    Takemoto, Y.2
  • 34
    • 33745683617 scopus 로고    scopus 로고
    • Recent progress in chiral Brønsted acid catalysis
    • Akiyama, T.; Itoh, J.; Fuchibe, K. Recent progress in chiral Brønsted acid catalysis. Adv. Synth. Catal. 2006, 348, 999-1010.
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 999-1010
    • Akiyama, T.1    Itoh, J.2    Fuchibe, K.3
  • 35
    • 38349189109 scopus 로고    scopus 로고
    • Stronger Brønsted acids
    • Akiyama, T. Stronger Brønsted acids. Chem. Rev. 2007, 107, 5744-5758.
    • (2007) Chem. Rev. , vol.107 , pp. 5744-5758
    • Akiyama, T.1
  • 36
    • 4143141139 scopus 로고    scopus 로고
    • In search of peptide-based catalysts for asymmetric organic synthesis
    • Miller, S. J. In search of peptide-based catalysts for asymmetric organic synthesis. Acc. Chem. Res. 2004, 37, 601-610.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 601-610
    • Miller, S.J.1
  • 37
    • 38349112828 scopus 로고    scopus 로고
    • Asymmetric catalysis mediated by synthetic peptides
    • Davie, E. A. C.; Mennen, S. M.; Xu, Y.; Miller, S. J. Asymmetric catalysis mediated by synthetic peptides. Chem. Rev. 2007, 107, 5759-5812.
    • (2007) Chem. Rev. , vol.107 , pp. 5759-5812
    • Davie, E.A.C.1    Mennen, S.M.2    Xu, Y.3    Miller, S.J.4
  • 38
    • 0037170944 scopus 로고    scopus 로고
    • Amino acids and peptides as asymmetric organocatalysts
    • Jarvo, E. R.; Miller, S. J. Amino acids and peptides as asymmetric organocatalysts. Tetrahedron 2002, 58, 2481-2495.
    • (2002) Tetrahedron , vol.58 , pp. 2481-2495
    • Jarvo, E.R.1    Miller, S.J.2
  • 39
    • 4143054678 scopus 로고    scopus 로고
    • Asymmetric organocatalysis of structurally welldefined chiral quaternary ammonium fluorides
    • Ooi, T.; Maruoka, K. Asymmetric organocatalysis of structurally welldefined chiral quaternary ammonium fluorides. Acc. Chem. Res. 2004, 37, 526-533.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 526-533
    • Ooi, T.1    Maruoka, K.2
  • 40
    • 4143063602 scopus 로고    scopus 로고
    • Asymmetric phase-transfer catalysis utilizing quaternary ammonium salts: Asymmetric alkylation of glycine imines
    • Lygo, B.; Andrews, B. I. Asymmetric phase-transfer catalysis utilizing quaternary ammonium salts: asymmetric alkylation of glycine imines. Acc. Chem. Res. 2004, 37, 518-525.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 518-525
    • Lygo, B.1    Andrews, B.I.2
  • 41
    • 38349148300 scopus 로고    scopus 로고
    • Recent development and application of chiral phase-transfer catalysts
    • Hashimoto, T.; Maruoka, K. Recent development and application of chiral phase-transfer catalysts. Chem. Rev. 2007, 107, 5656-5682.
    • (2007) Chem. Rev. , vol.107 , pp. 5656-5682
    • Hashimoto, T.1    Maruoka, K.2
  • 42
    • 0042880949 scopus 로고    scopus 로고
    • Enantioselective amino acid synthesis by chiral phase-transfer catalysis
    • Maruoka, K.; Ooi, T. Enantioselective amino acid synthesis by chiral phase-transfer catalysis. Chem. Rev. 2003, 103, 3013-3028.
    • (2003) Chem. Rev. , vol.103 , pp. 3013-3028
    • Maruoka, K.1    Ooi, T.2
  • 43
    • 85196432425 scopus 로고    scopus 로고
    • For reviews on catalytic asymmetric addition reactions to imines and related compounds
    • For reviews on catalytic asymmetric addition reactions to imines and related compounds see.
  • 44
    • 23844516156 scopus 로고    scopus 로고
    • Recent advances in catalytic asymmetric addition to imines and related com pounds
    • Vilaivan, T.; Bhanthumnavin, W.; Sritana-Anant, Y. Recent advances in catalytic asymmetric addition to imines and related com pounds. Curr. Org. Chem. 2005, 9, 1315-1392.
    • (2005) Curr. Org. Chem. , vol.9 , pp. 1315-1392
    • Vilaivan, T.1    Bhanthumnavin, W.2    Sritana-Anant, Y.3
  • 45
    • 34547796504 scopus 로고    scopus 로고
    • Catalytic, asymmetric alkylation of imines
    • Ferraris, D. Catalytic, asymmetric alkylation of imines. Tetrahedron 2007, 63, 9581-9597.
    • (2007) Tetrahedron , vol.63 , pp. 9581-9597
    • Ferraris, D.1
  • 46
    • 85196434939 scopus 로고    scopus 로고
    • For reviews on bifunctional organocatalysts see
    • For reviews on bifunctional organocatalysts see.
  • 47
    • 70349904154 scopus 로고    scopus 로고
    • Amide based bifunctional organocatalysts in asymmetric reactions
    • Liu, X. H.; Lin, L. L.; Feng, X. M. Amide based bifunctional organocatalysts in asymmetric reactions. Chem. Commun. 2009, 6145-6148.
    • (2009) Chem. Commun. , pp. 6145-6148
    • Liu, X.H.1    Lin, L.L.2    Feng, X.M.3
  • 48
    • 70349617279 scopus 로고    scopus 로고
    • Bifunctional chiral organocatalysts in organic transformations
    • Bhadury, P. S.; Song, B. A.; Yang, S.; Hu, D. Y.; Xue, W. Bifunctional chiral organocatalysts in organic transformations. Curr. Org. Chem. 2009, 6, 380-399.
    • (2009) Curr. Org. Chem. , vol.6 , pp. 380-399
    • Bhadury, P.S.1    Song, B.A.2    Yang, S.3    Hu, D.Y.4    Xue, W.5
  • 49
    • 61849117439 scopus 로고    scopus 로고
    • α,α- Diarylprolinols: Bifunctional organocatalysts for asymmetric synthesis
    • Lattanzi, A. α,α- Diarylprolinols: bifunctional organocatalysts for asymmetric synthesis. Chem. Commun. 2009, 1452-1463.
    • (2009) Chem. Commun. , pp. 1452-1463
    • Lattanzi, A.1
  • 50
    • 85196433879 scopus 로고    scopus 로고
    • For reviews on organocatalytic Mannich reactions see
    • For reviews on organocatalytic Mannich reactions see
  • 51
    • 1642415515 scopus 로고    scopus 로고
    • The direct catalytic asymmetric Mannich reaction
    • Córdova, A. The direct catalytic asymmetric Mannich reaction. Acc. Chem. Res. 2004, 37, 102-112.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 102-112
    • Córdova, A.1
  • 53
    • 85196433846 scopus 로고    scopus 로고
    • For reviews on organocatalyzed reactions with proline and derivatives see
    • For reviews on organocatalyzed reactions with proline and derivatives see.
  • 54
    • 4143114533 scopus 로고    scopus 로고
    • Enamine-based organocatalysis with proline and diamines: The development of direct catalytic asymmetric aldol, Mannich, Michael, and Diels-Alder reactions
    • Notz, W.; Tanaka, F.; Barbas III, C. F. Enamine-based organocatalysis with proline and diamines: The development of direct catalytic asymmetric aldol, Mannich, Michael, and Diels-Alder reactions. Acc. Chem. Res. 2004, 37, 580-591.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 580-591
    • Notz, W.1    Tanaka, F.2    Barbas III, C.F.3
  • 55
    • 45249123858 scopus 로고    scopus 로고
    • Organocatalytic asymmetric synthesis using proline and related molecules
    • Part 1
    • Kotsuki, H.; Ikishima, H.; Okuyama, A. Organocatalytic asymmetric synthesis using proline and related molecules. Part 1. Heterocycles 2008, 75, 493-529.
    • (2008) Heterocycles , vol.75 , pp. 493-529
    • Kotsuki, H.1    Ikishima, H.2    Okuyama, A.3
  • 56
    • 43849098896 scopus 로고    scopus 로고
    • Organocatalytic asymmetric synthesis using proline and related molecules
    • Part 2
    • Kotsuki, H.; Ikishima, H.; Okuyama, A. Organocatalytic asymmetric synthesis using proline and related molecules. Part 2. Heterocycles 2008, 75, 757-797.
    • (2008) Heterocycles , vol.75 , pp. 757-797
    • Kotsuki, H.1    Ikishima, H.2    Okuyama, A.3
  • 57
    • 47749137879 scopus 로고    scopus 로고
    • Supported proline and proline-derivatives as recyclable organocatalysts
    • Gruttadauria, M.; Giacalone, F.; Noto, R. Supported proline and proline-derivatives as recyclable organocatalysts. Chem. Soc. Rev. 2008, 37, 1666-1688.
    • (2008) Chem. Soc. Rev. , vol.37 , pp. 1666-1688
    • Gruttadauria, M.1    Giacalone, F.2    Noto, R.3
  • 58
    • 35348861428 scopus 로고    scopus 로고
    • Enantioselective aldol reaction: The blossoming of modern organocatalysis
    • Guillena, G.; Najera, C.; Ramon, D. J. Enantioselective aldol reaction: the blossoming of modern organocatalysis. Tetrahedron: Asymmetry 2007, 18, 2249-2293.
    • (2007) Tetrahedron: Asymmetry , vol.18 , pp. 2249-2293
    • Guillena, G.1    Najera, C.2    Ramon, D.J.3
  • 59
    • 0037028924 scopus 로고    scopus 로고
    • A Highly Enantioselective Amino Acid-Catalyzed Route to Functionalized - Amino Acids
    • Córdova, A.; Notz, W.; Zhong, G.; Betancort, J. M.; Barbas III, C. F. A Highly Enantioselective Amino Acid-Catalyzed Route to Functionalized - Amino Acids. J. Am. Chem. Soc. 2002, 124, 1842-1843.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 1842-1843
    • Córdova, A.1    Notz, W.2    Zhong, G.3    Betancort, J.M.4    Barbas III, C.F.5
  • 60
    • 0037028990 scopus 로고    scopus 로고
    • A highly enantioselective route to either enantiomer of both α- and β-amino acid derivatives
    • Córdova, A. Watanabe, S.; Tanaka, F.; Notz, W.; Barbas III, C. F. A highly enantioselective route to either enantiomer of both α- and β-amino acid derivatives. J. Am. Chem. Soc. 2002, 124, 1866-1867.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 1866-1867
    • Córdova, A.1    Watanabe, S.2    Tanaka, F.3    Notz, W.4    Barbas III, C.F.5
  • 62
    • 23944462365 scopus 로고    scopus 로고
    • Highly enantioselective synthesis of fluorinated γ-amino alcohols through proline-catalyzed cross-Mannich reaction
    • Fustero, S.; Jimenez, D.; Sanz-Cervera, J. F. S.; Sanchez-Roselo, M.; Esteban, E.; Simon-Fuentes, A. Highly enantioselective synthesis of fluorinated γ-amino alcohols through proline-catalyzed cross-Mannich reaction. Org. Lett. 2005, 7, 3433-3436.
    • (2005) Org. Lett. , vol.7 , pp. 3433-3436
    • Fustero, S.1    Jimenez, D.2    Sanz-Cervera, J.F.S.3    Sanchez-Roselo, M.4    Esteban, E.5    Simon-Fuentes, A.6
  • 63
    • 4043170073 scopus 로고    scopus 로고
    • Asymmetric synthesis of quaternary α- and β-amino acids and β-lactams via proline-catalyzed Mannich reactions with branched aldehyde donors
    • Chowdari, N. S.; Suri, J. T.; Barbas III, C. F. Asymmetric synthesis of quaternary α- and β-amino acids and β-lactams via proline-catalyzed Mannich reactions with branched aldehyde donors. Org. Lett. 2004, 6, 2507-2510.
    • (2004) Org. Lett. , vol.6 , pp. 2507-2510
    • Chowdari, N.S.1    Suri, J.T.2    Barbas III, C.F.3
  • 64
    • 31144436810 scopus 로고    scopus 로고
    • Proline-catalyzed, asymmetric Mannich reactions in the synthesis of a DPP-IV inhibitor
    • Janey, J. M.; Hsiao, Y.; Armstrong III, J. D. Proline-catalyzed, asymmetric Mannich reactions in the synthesis of a DPP-IV inhibitor. J. Org. Chem. 2006, 71, 390-392.
    • (2006) J. Org. Chem. , vol.71 , pp. 390-392
    • Janey, J.M.1    Hsiao, Y.2    Armstrong III, J.D.3
  • 65
    • 52949138243 scopus 로고    scopus 로고
    • Enantioselective organocatalytic Mannich reactions of ferrocenecarbaldehyde
    • Valero, G.; Balaguer, A.-N.; Moyano, A.; Rios, R. Enantioselective organocatalytic Mannich reactions of ferrocenecarbaldehyde. Tetrahedron Lett. 2008, 49, 6559-6562.
    • (2008) Tetrahedron Lett , vol.49 , pp. 6559-6562
    • Valero, G.1    Balaguer, A.-N.2    Moyano, A.3    Rios, R.4
  • 66
    • 0034721440 scopus 로고    scopus 로고
    • The direct catalytic asymmetric three-component Mannich reaction
    • List, B. The direct catalytic asymmetric three-component Mannich reaction. J. Am. Chem. Soc. 2000, 122, 9336-9337.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9336-9337
    • List, B.1
  • 67
    • 0037028550 scopus 로고    scopus 로고
    • The proline-catalyzed direct asymmetric threecomponent Mannich reaction: Scope, optimization, and opplication to the highly enantioselective synthesis of 1,2-amino alcohols
    • List, B.; Pojarliev, P.; Biller, W. T.; Martin, H. J. The proline-catalyzed direct asymmetric threecomponent Mannich reaction: Scope, optimization, and opplication to the highly enantioselective synthesis of 1,2-amino alcohols. J. Am. Chem. Soc. 2002, 124, 827-833.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 827-833
    • List, B.1    Pojarliev, P.2    Biller, W.T.3    Martin, H.J.4
  • 69
    • 33746606463 scopus 로고    scopus 로고
    • 3-Pyrrolidinecarboxylic acid for direct catalytic asymmetric anti-Mannich-type reactions of unmodified ketones
    • Zhang, H.; Mifsud, M.; Tanaka, F.; Barbas III, C. F. 3-Pyrrolidinecarboxylic acid for direct catalytic asymmetric anti-Mannich-type reactions of unmodified ketones. J. Am. Chem. Soc. 2006, 128, 9630-9631.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 9630-9631
    • Zhang, H.1    Mifsud, M.2    Tanaka, F.3    Barbas III, C.F.4
  • 70
    • 0038262875 scopus 로고    scopus 로고
    • Origins of opposite absolute stereoselectivities in proline-catalyzed direct Mannich and aldol reactions
    • Bahmanyar, S.; Houk, K. N. Origins of opposite absolute stereoselectivities in proline-catalyzed direct Mannich and aldol reactions. Org. Lett. 2003, 5, 1249-1251.
    • (2003) Org. Lett. , vol.5 , pp. 1249-1251
    • Bahmanyar, S.1    Houk, K.N.2
  • 71
    • 71749091655 scopus 로고    scopus 로고
    • Theoretical studies of stereoselectivities in the direct organocatalytic Mannich reactions involving ketimine
    • Li, H.; Fu, A.; Shi, H. Theoretical studies of stereoselectivities in the direct organocatalytic Mannich reactions involving ketimine. J. Mol. Cat. A 2009, 303, 1-8.
    • (2009) J. Mol. Cat. A. , vol.303 , pp. 1-8
    • Li, H.1    Fu, A.2    Shi, H.3
  • 72
    • 57449089357 scopus 로고    scopus 로고
    • Theoretical investigations on the stereoselectivity of the proline catalyzed Mannich reaction in DMSO
    • Parasuk, W.; Parasuk, V. Theoretical investigations on the stereoselectivity of the proline catalyzed Mannich reaction in DMSO. J. Org. Chem. 2008, 73, 9388-9392.
    • (2008) J. Org. Chem. , vol.73 , pp. 9388-9392
    • Parasuk, W.1    Parasuk, V.2
  • 73
    • 38349089956 scopus 로고    scopus 로고
    • Catalysis of 3-pyrrolidinecarboxylic acid and related pyrrolidine derivatives in enantioselective anti-Mannich-type reactions: Importance of the 3-acid group on pyrrolidine for sterecontrol
    • Zhang, H.; Mitsumori, S.; Utsumi, N.; Imai, M.; Garcia-Delgado, N.; Mifsud, M.; Albertshofer, K.; Cheon, P. H.-Y.; Houk, K. N.; Tanaka, F.; Barbas III, C. F. Catalysis of 3-pyrrolidinecarboxylic acid and related pyrrolidine derivatives in enantioselective anti-Mannich-type reactions: Importance of the 3-acid group on pyrrolidine for sterecontrol. J. Am. Chem. Soc. 2008, 130, 875-886.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 875-886
    • Zhang, H.1    Mitsumori, S.2    Utsumi, N.3    Imai, M.4    Garcia-Delgado, N.5    Mifsud, M.6    Albertshofer, K.7    Cheon P., H.-Y.8    Houk, K.N.9    Tanaka, F.10    Barbas III, C.F.11
  • 74
    • 34249888744 scopus 로고    scopus 로고
    • Acyclic β-amino acid catalyzed asymmetric antiselective Mannich-type reactions
    • Dziedzic, P.; Córdova, A. Acyclic β-amino acid catalyzed asymmetric antiselective Mannich-type reactions. Tetrahedron Lett. 2007, 18, 1033-1037.
    • (2007) Tetrahedron Lett , vol.18 , pp. 1033-1037
    • Dziedzic, P.1    Córdova, A.2
  • 75
    • 33846198424 scopus 로고    scopus 로고
    • Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactions
    • Ramasastry, S. S. V.; Zhang, H.; Tanaka, F.; Barbas III, C. F. Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactions. J. Am. Chem. Soc. 2007, 129, 288-289.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 288-289
    • Ramasastry, S.S.V.1    Zhang, H.2    Tanaka, F.3    Barbas III, C.F.4
  • 76
    • 84954358740 scopus 로고    scopus 로고
    • Theoretical studies of stereoselectivities in the direct syn- and anti-Mannich reactions catalyzed by different amino acids Tetrahedron
    • Fu, A.; Li, H.; Si, H.; Yuan, S.; Duan, Y. Theoretical studies of stereoselectivities in the direct syn- and anti-Mannich reactions catalyzed by different amino acids Tetrahedron: Asymmetry 2008, 19, 2285-2292.
    • (2008) Asymmetry , vol.19 , pp. 2285-2292
    • Fu, A.1    Li, H.2    Si, H.3    Yuan, S.4    Duan, Y.5
  • 78
    • 50649103777 scopus 로고    scopus 로고
    • Organocatalytic anti-Mannich reactions with dihydroxyacetone and acyclic dihydroxyacetone derivatives: A facile route to amino sugars
    • Zhang, H.; Ramasastry, S. S. V.; Tanaka, F.; Barbas III, C. F. Organocatalytic anti-Mannich reactions with dihydroxyacetone and acyclic dihydroxyacetone derivatives: A facile route to amino sugars. Adv. Synth. Catal. 2008, 350, 791-796.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 791-796
    • Zhang, H.1    Ramasastry, S.S.V.2    Tanaka, F.3    Barbas III, C.F.4
  • 79
    • 37649024285 scopus 로고    scopus 로고
    • Direct catalytic asymmetric threecomponent Mannich reactions with dihydroxyacetone: Enantioselective synthesis of amino sugar derivatives
    • Dziedzic, P.; Ibrahem, I.; Córdova, A. Direct catalytic asymmetric threecomponent Mannich reactions with dihydroxyacetone: enantioselective synthesis of amino sugar derivatives. Tetrahedron Lett. 2008, 49, 803-807.
    • (2008) Tetrahedron Lett , vol.49 , pp. 803-807
    • Dziedzic, P.1    Ibrahem, I.2    Córdova, A.3
  • 80
    • 71049138987 scopus 로고    scopus 로고
    • One-pot highly enantioselective catalytic Mannich-type reactions between aldehydes and stable α-amido sulfones: Asymmetric synthesis of β-amino aldehydes and β-aminoacids
    • Deiana, L.; Zhao, G.-L.; Dziedzic, P.; Rios, R.; Vesely, J.; Ekstrom, J.; Córdova, A. One-pot highly enantioselective catalytic Mannich-type reactions between aldehydes and stable α-amido sulfones: asymmetric synthesis of β-amino aldehydes and β-aminoacids. Tetrahedron Lett. 2010, 51, 234-237.
    • (2010) Tetrahedron Lett , vol.51 , pp. 234-237
    • Deiana, L.1    Zhao, G.-L.2    Dziedzic, P.3    Rios, R.4    Vesely, J.5    Ekstrom, J.6    Córdova, A.7
  • 81
    • 64249148782 scopus 로고    scopus 로고
    • Enantioselective Mannich reactions with the practical proline mimetic N-(p-dodecylphenyl-sulfonyl)-2-pyrrolidinecarboxamide
    • Yang, H.; Carter, R. G. Enantioselective Mannich reactions with the practical proline mimetic N-(p-dodecylphenyl-sulfonyl)-2-pyrrolidinecarboxamide. J. Org. Chem. 2009, 74, 2246-2249.
    • (2009) J. Org. Chem. , vol.74 , pp. 2246-2249
    • Yang, H.1    Carter, R.G.2
  • 82
    • 51749116225 scopus 로고    scopus 로고
    • 3- Trifluoromethanesulfonamido-pyrrolidine: A general organocatalyst for antiselective Mannich reactions
    • Pouliquen, M.; Blanchet, J.; Lasne, M.-C.; Rouden J. 3- Trifluoromethanesulfonamido-pyrrolidine: A general organocatalyst for antiselective Mannich reactions. Org. Lett. 2008, 10, 1029-1032.
    • (2008) Org. Lett. , vol.10 , pp. 1029-1032
    • Pouliquen, M.1    Blanchet, J.2    Lasne, M.-C.3    Rouden, J.4
  • 83
    • 37349005457 scopus 로고    scopus 로고
    • Organocatalytic asymmetric Mannich reactions: New methodology, catalyst, design and synthetic applications
    • Ting, A.; Schaus, S. E. Organocatalytic asymmetric Mannich reactions: New methodology, catalyst, design and synthetic applications. Eur. J. Org. Chem. 2007, 5797-5815.
    • (2007) Eur. J. Org. Chem. , pp. 5797-5815
    • Ting, A.1    Schaus, S.E.2
  • 84
    • 28444445588 scopus 로고    scopus 로고
    • anti-Selective direct asymmetric Mannich reactions catalyzed by axially chiral amino sulfonamide as an organocatalyst
    • Kano, T.; Yamaguchi, Y.; Tokuda, O.; Maruoka, K. anti-Selective direct asymmetric Mannich reactions catalyzed by axially chiral amino sulfonamide as an organocatalyst. J. Am. Chem. Soc. 2005, 127, 16408-16409.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 16408-16409
    • Kano, T.1    Yamaguchi, Y.2    Tokuda, O.3    Maruoka, K.4
  • 85
    • 71749088922 scopus 로고    scopus 로고
    • Theoretical studies of stereoselectivities in the direct anti-Mannich and syn-aldol reactions catalyzed by axially chiral amino sulfonamide
    • Fu, A.; Li, H.; Chu, T.; Zou, H.; Feng, P.; Yuan, S.; Duan, Y. Theoretical studies of stereoselectivities in the direct anti-Mannich and syn-aldol reactions catalyzed by axially chiral amino sulfonamide. J. Mol. Cat. A. 2009, 314, 1-8.
    • (2009) J. Mol. Cat. A. , vol.314 , pp. 1-8
    • Fu, A.1    Li, H.2    Chu, T.3    Zou, H.4    Feng, P.5    Yuan, S.6    Duan, Y.7
  • 86
    • 85196434485 scopus 로고    scopus 로고
    • For reviews on catalytic asymmetric Strecker reactions see
    • For reviews on catalytic asymmetric Strecker reactions see.
  • 88
    • 0041378065 scopus 로고    scopus 로고
    • Catalytic enantioselective Strecker reactions and analogous synthesis
    • Gröger, H. Catalytic enantioselective Strecker reactions and analogous synthesis. Chem. Rev. 2003, 103, 2795-2827.
    • (2003) Chem. Rev. , vol.103 , pp. 2795-2827
    • Gröger, H.1
  • 89
    • 0033564990 scopus 로고    scopus 로고
    • Enantioselective synthesis of α-amino nitriles from N-benzhydryl imines and HCN with a chiral bicyclic guanidine as catalyst
    • Corey, E. J.; Grogan, M. J. Enantioselective synthesis of α-amino nitriles from N-benzhydryl imines and HCN with a chiral bicyclic guanidine as catalyst. Org. Lett. 1999, 1, 157-160.
    • (1999) Org. Lett. , vol.1 , pp. 157-160
    • Corey, E.J.1    Grogan, M.J.2
  • 90
    • 0029990764 scopus 로고    scopus 로고
    • Asymmetric catalysis of the Strecker amino acid synthesis by a cyclic dipeptide
    • Iyer, M. S.; Gigstad, K. M.; Namdev, N. D.; Lipton, M. Asymmetric catalysis of the Strecker amino acid synthesis by a cyclic dipeptide. J. Am. Chem. Soc. 1996, 118, 4910-4911.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 4910-4911
    • Iyer, M.S.1    Gigstad, K.M.2    Namdev, N.D.3    Lipton, M.4
  • 91
    • 49249103067 scopus 로고    scopus 로고
    • Organocatalytic enantioselective hydrophosphonylation of sulfonylimines having a heteroarenesulfonyl group as a novel stereocontroller
    • Nakamura, S.; Nakashima, H.; Yamamura, A.; Shibata, N.; Toru, T. Organocatalytic enantioselective hydrophosphonylation of sulfonylimines having a heteroarenesulfonyl group as a novel stereocontroller. Adv. Synth. Catal. 2008, 305, 1209-1212.
    • (2008) Adv. Synth. Catal. , vol.305 , pp. 1209-1212
    • Nakamura, S.1    Nakashima, H.2    Yamamura, A.3    Shibata, N.4    Toru, T.5
  • 92
    • 85196435807 scopus 로고    scopus 로고
    • For a review on the catalytic asymmetric Pudovik reaction see
    • For a review on the catalytic asymmetric Pudovik reaction see
  • 93
    • 49249117085 scopus 로고    scopus 로고
    • Catalytic enantioselective hydrophosphonylation of aldehydes and imines
    • Merino, P.; Marques-Lopez, E.; Herrera, R. P. Catalytic enantioselective hydrophosphonylation of aldehydes and imines. Adv. Synth. Catal. 2008, 350, 1195-1208.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 1195-1208
    • Merino, P.1    Marques-Lopez, E.2    Herrera, R.P.3
  • 94
    • 73249115987 scopus 로고    scopus 로고
    • Catalytic enantioselective hydrophosphonylation of ketimines using cinchona alkaloids
    • Nakamura, S.; Hayashi, M.; Hiramatsu, Y.; Shibata, N.; Funahashi, Y.; Toru, T. Catalytic enantioselective hydrophosphonylation of ketimines using cinchona alkaloids. J. Am. Chem. Soc. 2009, 131, 18240-18241.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 18240-18241
    • Nakamura, S.1    Hayashi, M.2    Hiramatsu, Y.3    Shibata, N.4    Funahashi, Y.5    Toru, T.6
  • 95
    • 72149086659 scopus 로고    scopus 로고
    • Organocatalytic asymmetric synthesis of protected α,β-diamino acids
    • Shi, Z.; Yu, P.; Chua, P. J.; Zhong, G. Organocatalytic asymmetric synthesis of protected α,β-diamino acids. Adv. Synth. Catal. 2009, 351, 2797-2800.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 2797-2800
    • Shi, Z.1    Yu, P.2    Chua, P.J.3    Zhong, G.4
  • 96
    • 23844490047 scopus 로고    scopus 로고
    • Asymmetric Mannich reactions of β-keto esters with acyl imines catalyzed by cinchona alkaloids
    • Lou, S.; Taoka, B. M.; Ting, A.; Schaus, S. E. Asymmetric Mannich reactions of β-keto esters with acyl imines catalyzed by cinchona alkaloids. J. Am. Chem. Soc. 2005, 127, 11256-11257.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 11256-11257
    • Lou, S.1    Taoka, B.M.2    Ting, A.3    Schaus, S.E.4
  • 97
    • 54049122287 scopus 로고    scopus 로고
    • Organocatalytic Mannich-type reactions of trifluoroethyl thioesters
    • Utsumi, N.; Kitagaki, S.; Barbas III, C. F. Organocatalytic Mannich-type reactions of trifluoroethyl thioesters. Org. Lett. 2008, 10, 3405-3408.
    • (2008) Org. Lett. , vol.10 , pp. 3405-3408
    • Utsumi, N.1    Kitagaki, S.2    Barbas III C.F3
  • 98
    • 34548249167 scopus 로고    scopus 로고
    • Aza-Morita-Baylis-Hillman-type reactions: Highly enantioselective organocatalytic addition of unmodified α,β- unsaturated aldehydes to N-Boc protected imines
    • Vesely, J.; Dziedzic, P.; Córdova, A. Aza-Morita-Baylis-Hillman-type reactions: highly enantioselective organocatalytic addition of unmodified α,β- unsaturated aldehydes to N-Boc protected imines. Tetrahedron Lett. 2007, 48, 6900-6904.
    • (2007) Tetrahedron Lett , vol.48 , pp. 6900-6904
    • Vesely, J.1    Dziedzic, P.2    Córdova, A.3
  • 99
    • 53149135050 scopus 로고    scopus 로고
    • Catalytic asymmetric synthesis of the docetaxel (Taxotere) side chain: Organocatalytic highly enantioselective synthesis of esterification-ready α-hydroxy-β-amino acids
    • Dziedzic, P.; Vesely, J.; Córdova, A. Catalytic asymmetric synthesis of the docetaxel (Taxotere) side chain: organocatalytic highly enantioselective synthesis of esterification-ready α-hydroxy-β-amino acids. Tetrahedron Lett. 2008, 49, 6631-6634.
    • (2008) Tetrahedron Lett , vol.49 , pp. 6631-6634
    • Dziedzic, P.1    Vesely, J.2    Córdova, A.3
  • 100
    • 29844448114 scopus 로고    scopus 로고
    • Recognition and activation by ureas and thioureas: Stereoselective reactions using ureas and thioureas as hydrogen-bonding donors
    • Takemoto, Y. Recognition and activation by ureas and thioureas: stereoselective reactions using ureas and thioureas as hydrogen-bonding donors. Org. Biomol. Chem. 2005, 3, 4299-4306.
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 4299-4306
    • Takemoto, Y.1
  • 101
    • 33746277515 scopus 로고    scopus 로고
    • Organocatalysis mediated by (thio)urea derivatives
    • Connon, S. J. Organocatalysis mediated by (thio)urea derivatives. Chem. Eur. J. 2006, 12, 5418-5427.
    • (2006) Chem. Eur. J. , vol.12 , pp. 5418-5427
    • Connon, S.J.1
  • 102
    • 77951669558 scopus 로고    scopus 로고
    • The design of chiral double hydrogen bonding networks and their applications to catalytic asymmetric carbon-carbon and carbon-oxygen bond-forming reactions
    • Sohtome, Y.; Nagasawa, K. The design of chiral double hydrogen bonding networks and their applications to catalytic asymmetric carbon-carbon and carbon-oxygen bond-forming reactions. Synlett 2010, 1-22.
    • (2010) Synlett , pp. 1-22
    • Sohtome, Y.1    Nagasawa, K.2
  • 103
    • 38049089797 scopus 로고    scopus 로고
    • Enantioselective organocatalytic transfer hydrogenation reactions using Hatzsch esters
    • For a review see
    • For a review see: Ouellet, S. G.; Walji, A. M.; MacMillan, D. W. C. Enantioselective organocatalytic transfer hydrogenation reactions using Hatzsch esters. Acc. Chem. Res. 2007, 40, 1327-1339.
    • (2007) Acc. Chem. Res. , vol.40 , pp. 1327-1339
    • Ouellet, S.G.1    Walji, A.M.2    Macmillan, D.W.C.3
  • 104
    • 33645755227 scopus 로고    scopus 로고
    • Thiourea catalyzed direct reductive amination of aldehydes
    • Menche, D.; Arikan, F. Thiourea catalyzed direct reductive amination of aldehydes. Synlett 2006, 841-844.
    • (2006) Synlett , pp. 841-844
    • Menche, D.1    Arikan, F.2
  • 106
    • 0037189898 scopus 로고    scopus 로고
    • Structure-based analysis and optimization of a highly enantioselective catalyst for the Strecker reaction
    • Vachal, P.; Jacobsen, E. N. Structure-based analysis and optimization of a highly enantioselective catalyst for the Strecker reaction. J. Am. Chem. Soc. 2002, 124, 10012-10013.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10012-10013
    • Vachal, P.1    Jacobsen, E.N.2
  • 107
    • 38049089797 scopus 로고    scopus 로고
    • Enantioselective organocatalytic transfer hydrogenation reactions using Hantzsch esters
    • Ouellet, S. G.; Walji, A. M.; MacMillan, D. W. C. Enantioselective organocatalytic transfer hydrogenation reactions using Hantzsch esters. Acc. Chem. Res. 2007, 40, 1327-1339.
    • (2007) Acc. Chem. Res. , vol.40 , pp. 1327-1339
    • Ouellet, S.G.1    Walji, A.M.2    Macmillan, D.W.C.3
  • 108
    • 68049101352 scopus 로고    scopus 로고
    • Organocatalytic highly enantio- and diastereoselective Mannich reaction of β-ketoesters with N-Boc aldimines
    • Kang, Y. K.; Kim, D. Y. Organocatalytic highly enantio- and diastereoselective Mannich reaction of β-ketoesters with N-Boc aldimines. J. Org. Chem. 2009, 74, 5734-5737.
    • (2009) J. Org. Chem. , vol.74 , pp. 5734-5737
    • Kang, Y.K.1    Kim, D.Y.2
  • 109
    • 33847331148 scopus 로고    scopus 로고
    • Organocatalytic and highly stereoselective direct vinylogous Mannich reaction
    • Liu, T. Y.; Cui, H.-L.; Long, J.; Li, B.-J.; Wu, Y.; Ding, L.-S.; Chen, Y.- C. Organocatalytic and highly stereoselective direct vinylogous Mannich reaction. J. Am. Chem. Soc. 2007, 129, 1878-1879.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 1878-1879
    • Liu, T.Y.1    Cui, H.-L.2    Long, J.3    Li, B.-J.4    Wu, Y.5    Ding, L.-S.6    Chen Y.-, C.7
  • 110
    • 54049101193 scopus 로고    scopus 로고
    • Organocatalytic stereoselective Mannich reaction of 3-substituted oxindoles
    • 3583-2586
    • Tian, X.; Jiang, K.; Peng, J.; Du, W.; Chen, Y.-C. Organocatalytic stereoselective Mannich reaction of 3-substituted oxindoles. Org. Lett. 2008, 10, 3583-2586.
    • (2008) Org. Lett. , vol.10
    • Tian, X.1    Jiang, K.2    Peng, J.3    Du, W.4    Chen, Y.-C.5
  • 112
    • 0037032312 scopus 로고    scopus 로고
    • Asymmetric catalytic Mannich reactions catalyzed by urea derivatives: Enantioselective synthesis of β -aryl- β -amino acids
    • Wenzel, A. G.; Jacobsen, E. N. Asymmetric catalytic Mannich reactions catalyzed by urea derivatives: Enantioselective synthesis of β -aryl- β -amino acids. J. Am. Chem. Soc. 2002, 124, 12965-12966.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 12965-12966
    • Wenzel, A.G.1    Jacobsen, E.N.2
  • 113
    • 33646511310 scopus 로고    scopus 로고
    • The Mannich reactions of malonates with simple imines catalyzed by bifunctional Cinchona alkaloids: Enantioselective synthesis of β-amino acids
    • Song, J.; Wang, Y.; Deng, L. The Mannich reactions of malonates with simple imines catalyzed by bifunctional Cinchona alkaloids: Enantioselective synthesis of β-amino acids. J. Am. Chem. Soc. 2006, 128, 6048-6049.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 6048-6049
    • Song, J.1    Wang, Y.2    Deng, L.3
  • 114
    • 85196434282 scopus 로고    scopus 로고
    • For a review on catalytic asymmetric aza-Henry reactions see
    • For a review on catalytic asymmetric aza-Henry reactions see
  • 116
    • 12344267138 scopus 로고    scopus 로고
    • Highly enantioselective thiourea-catalyzed nitro-Mannich reaction
    • Toon, T. P.; Jacobsen, E. N. Highly enantioselective thiourea-catalyzed nitro-Mannich reaction. Angew. Chem. Int. Ed. 2005, 44, 466-468.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 466-468
    • Toon, T.P.1    Jacobsen, E.N.2
  • 117
    • 46949091946 scopus 로고    scopus 로고
    • Novel bifunctional chiral thiourea catalyzed highly enantioselective aza-Henry reaction
    • Wang, C.; Zhou, Z.; Tang, C. Novel bifunctional chiral thiourea catalyzed highly enantioselective aza-Henry reaction. Org. Lett. 2008, 10, 1707-1710.
    • (2008) Org. Lett. , vol.10 , pp. 1707-1710
    • Wang, C.1    Zhou, Z.2    Tang, C.3
  • 118
    • 60849111107 scopus 로고    scopus 로고
    • Enantioselective aza-Henry reaction with acyclic guanidine-thiourea bifunctional organocatalyst
    • Takada, K.; Nagasawa, K. Enantioselective aza-Henry reaction with acyclic guanidine-thiourea bifunctional organocatalyst. Adv. Synth. Catal. 2009, 351, 345-347.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 345-347
    • Takada, K.1    Nagasawa, K.2
  • 119
    • 70349416551 scopus 로고    scopus 로고
    • Doubly stereocontrolled asymmetric aza-Henry reaction with in situ generation of N-Boc-imines catalyzed by novel rosin-derived amine thiourea catalysts
    • Jiang, X.; Zhang, Y.; Wu, L.; Zhang, G.; Liu, X.; Zhang, H.; Fu, D.; Wang, R. Doubly stereocontrolled asymmetric aza-Henry reaction with in situ generation of N-Boc-imines catalyzed by novel rosin-derived amine thiourea catalysts. Adv. Synth. Catal. 2009, 351, 2096-2100.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 2096-2100
    • Jiang, X.1    Zhang, Y.2    Wu, L.3    Zhang, G.4    Liu, X.5    Zhang, H.6    Fu, D.7    Wang, R.8
  • 120
    • 0034601025 scopus 로고    scopus 로고
    • Nitronate anion recognition and modulation of ambident reactivity by hydrogen-bonding receptors
    • Linton, B. R.; Goodman, M. S.; Hamilton, A. D. Nitronate anion recognition and modulation of ambident reactivity by hydrogen-bonding receptors. Chem. Eur. J. 2000, 6, 2449-2455.
    • (2000) Chem. Eur. J. , vol.6 , pp. 2449-2455
    • Linton, B.R.1    Goodman, M.S.2    Hamilton, A.D.3
  • 121
    • 0142072631 scopus 로고    scopus 로고
    • Enantioselective Michael reaction of malonates to nitroolefins catalyzed by bifunctional organocatalysts
    • Okino, N.; Hoashi, Y.; Takemoto, Y. Enantioselective Michael reaction of malonates to nitroolefins catalyzed by bifunctional organocatalysts. J. Am. Chem. Soc. 2003, 125, 12672-12673.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 12672-12673
    • Okino, N.1    Hoashi, Y.2    Takemoto, Y.3
  • 122
    • 1342268984 scopus 로고    scopus 로고
    • Enantioselective aza-Henry reaction catalyzed by a bifunctional organocatalyst
    • Okino, T.; Nakamura, S.; Furukawa, T.; Takemoto, Y. Enantioselective aza-Henry reaction catalyzed by a bifunctional organocatalyst. Org. Lett. 2004, 6, 625-627.
    • (2004) Org. Lett. , vol.6 , pp. 625-627
    • Okino, T.1    Nakamura, S.2    Furukawa, T.3    Takemoto, Y.4
  • 123
    • 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
  • 124
    • 68149144269 scopus 로고    scopus 로고
    • Diastereo- and enantioselective aza-MBH-type reaction of nitroalkenes to N-tosylimines catalyzed by functional organocatalysts
    • Wang, X.; Chen, Y.-F.; Niu, L.-F.; Xu, P.-F. Diastereo- and enantioselective aza-MBH-type reaction of nitroalkenes to N-tosylimines catalyzed by functional organocatalysts. Org. Lett. 2009, 11, 3310-3313.
    • (2009) Org. Lett. , vol.11 , pp. 3310-3313
    • Wang, X.1    Chen, Y.-F.2    Niu, L.-F.3    Xu, P.-F.4
  • 125
    • 67649403306 scopus 로고    scopus 로고
    • Trifunctional organocatalyst-promoted counterion catalysis for fast and enantioselective aza-Morita-Baylis-Hillman reactions at ambient temperature
    • Garnier, J.-M.; Liu, F. Trifunctional organocatalyst-promoted counterion catalysis for fast and enantioselective aza-Morita-Baylis-Hillman reactions at ambient temperature. Org. Biomol. Chem. 2009, 1272-1275.
    • (2009) Org. Biomol. Chem. , pp. 1272-1275
    • Garnier, J.-M.1    Liu, F.2
  • 126
    • 1842555199 scopus 로고    scopus 로고
    • Thiourea-catalyzed enantioselective hydrophoshonylation of imines: Practical access to enantiomerically enriched - amino phosphonic acids
    • Joly, G. D.; Jacobsen, E. N. Thiourea-catalyzed enantioselective hydrophoshonylation of imines: Practical access to enantiomerically enriched - amino phosphonic acids. J. Am. Chem. Soc. 2004, 126, 4102-4103.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 4102-4103
    • Joly, G.D.1    Jacobsen, E.N.2
  • 127
    • 0034599654 scopus 로고    scopus 로고
    • A general catalyst for the asymmetric Strecker reaction
    • Sigman, M. S.; Vachal, P.; Jacobsen, E. N. A general catalyst for the asymmetric Strecker reaction. Angew. Chem. Int. Ed. 2000, 39, 1279-1281.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1279-1281
    • Sigman, M.S.1    Vachal, P.2    Jacobsen, E.N.3
  • 128
    • 0034704642 scopus 로고    scopus 로고
    • Enantioselective catalytic addition of HCN to ketoimines. Catalytic synthesis of quaternary amino acids
    • Vachal, P.; Jacobsen, E. N. Enantioselective catalytic addition of HCN to ketoimines. Catalytic synthesis of quaternary amino acids. Org. Lett. 2000, 2, 867-870.
    • (2000) Org. Lett. , vol.2 , pp. 867-870
    • Vachal, P.1    Jacobsen, E.N.2
  • 129
    • 0037189898 scopus 로고    scopus 로고
    • Structure-based analysis and optimization of a highly enantioselective catalyst for the Strecker reaction
    • Vachal, P.; Jacobsen, E. N. Structure-based analysis and optimization of a highly enantioselective catalyst for the Strecker reaction. J. Am. Chem. Soc. 2002, 124, 10012-10014.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10012-10014
    • Vachal, P.1    Jacobsen, E.N.2
  • 130
    • 85196435631 scopus 로고    scopus 로고
    • For recent reviews see
    • For recent reviews see.
  • 131
    • 73049097100 scopus 로고    scopus 로고
    • The role of the indole in important organocatalytic enantioselective Friedel-Crafts alkylation reactions
    • Marqués-López, E.; Diez-Martínez, A.; Merino, P.; Herrera, R. P. The role of the indole in important organocatalytic enantioselective Friedel-Crafts alkylation reactions. Curr. Org. Chem. 2009, 13, 1585-1609.
    • (2009) Curr. Org. Chem. , vol.13 , pp. 1585-1609
    • Marqués-López, E.1    Diez-Martínez, A.2    Merino, P.3    Herrera, R.P.4
  • 132
    • 1042276935 scopus 로고    scopus 로고
    • New catalytic approaches in the stereoselective Friedel-Crafts alkylation reaction
    • Bandini, M.; Melloni, A.; Umani-Ronchi, A. New catalytic approaches in the stereoselective Friedel-Crafts alkylation reaction. Angew. Chem., Int. Ed. 2004, 43, 550-556.
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 550-556
    • Bandini, M.1    Melloni, A.2    Umani-Ronchi, A.3
  • 133
    • 0037680718 scopus 로고    scopus 로고
    • Asymmetric Friedel- Crafts reactions: Catalytic enantioselective adddition of aromatic and heteroaromatic C-H bonds to activated alkenes, carbonyl compounds and imines
    • Jørgensen, K. A. Asymmetric Friedel- Crafts reactions: Catalytic enantioselective adddition of aromatic and heteroaromatic C-H bonds to activated alkenes, carbonyl compounds and imines. Synthesis 2003, 1117-1125.
    • (2003) Synthesis , pp. 1117-1125
    • Jørgensen, K.A.1
  • 134
    • 33745672062 scopus 로고    scopus 로고
    • Asymmetric Friedel-Crafts reaction of indoles with imines by an organic catalyst
    • Wang, Y.-Q.; Song, J.; Hong, R.; Li, H.; Deng, L. Asymmetric Friedel-Crafts reaction of indoles with imines by an organic catalyst. J. Am. Chem. Soc. 2006, 128, 8156-8157.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 8156-8157
    • Wang, Y.-Q.1    Song, J.2    Hong, R.3    Li, H.4    Deng, L.5
  • 135
    • 85196432777 scopus 로고    scopus 로고
    • For reviews on allylation of imines and related compounds see
    • For reviews on allylation of imines and related compounds see.
  • 136
    • 33646469171 scopus 로고    scopus 로고
    • Stereoselective allylation reactions of imines and related compounds
    • Merino, P.; Tejero, T.; Delso, I.; Mannucci, V. Stereoselective allylation reactions of imines and related compounds. Curr. Org. Synth. 2005, 2, 479-498.
    • (2005) Curr. Org. Synth. , vol.2 , pp. 479-498
    • Merino, P.1    Tejero, T.2    Delso, I.3    Mannucci, V.4
  • 137
    • 27944492745 scopus 로고    scopus 로고
    • Asymmetric addition of allylic nucleophiles to imino compounds
    • Ding, H.; Friedstad, G. K. Asymmetric addition of allylic nucleophiles to imino compounds. Synthesis 2005, 2815-2829.
    • (2005) Synthesis , pp. 2815-2829
    • Ding, H.1    Friedstad, G.K.2
  • 138
    • 34247164504 scopus 로고    scopus 로고
    • Indium-mediated asymmetric allylation of acylhydrazones using a chiral urea catalyst
    • Tan, K. L.; Jacobsen, E. N. Indium-mediated asymmetric allylation of acylhydrazones using a chiral urea catalyst. Angew. Chem. Int. Ed. 2007, 46, 1315-1317.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1315-1317
    • Tan, K.L.1    Jacobsen, E.N.2
  • 139
    • 85196434884 scopus 로고    scopus 로고
    • For reviews on nucleophilic additions to nitrones see
    • For reviews on nucleophilic additions to nitrones see.
  • 140
    • 18744403152 scopus 로고    scopus 로고
    • Nitrones and its cyclic analogues In Science of Synthesis
    • Thieme Verlag. New York, Padwa, A. (Ed.)
    • Merino, P. Nitrones and its cyclic analogues In Science of Synthesis. Georg. Thieme Verlag. New York. Vol. 27, Padwa, A. (Ed.). 2004, 511-580.
    • (2004) Georg , vol.27 , pp. 511-580
    • Merino, P.1
  • 141
    • 0034112410 scopus 로고    scopus 로고
    • Nucleophilic additions to chiral nitrones: New approaches to nitrogenated compounds
    • Merino, P.; Franco, S.; Merchan, F. L.; Tejero, T. Nucleophilic additions to chiral nitrones: New approaches to nitrogenated compounds. Synlett 2000, 442-454.
    • (2000) Synlett , pp. 442-454
    • Merino, P.1    Franco, S.2    Merchan, F.L.3    Tejero, T.4
  • 142
    • 0037474640 scopus 로고    scopus 로고
    • Thiourea-catalyzed nucleophilic addition of TMSCN and ketene silyl acetals to nitrones and aldehydes
    • Okino, T.; Hoashi, Y.; Takemoto, Y. Thiourea-catalyzed nucleophilic addition of TMSCN and ketene silyl acetals to nitrones and aldehydes. Tetrahedron Lett. 2003, 44, 2817-2821.
    • (2003) Tetrahedron Lett , vol.44 , pp. 2817-2821
    • Okino, T.1    Hoashi, Y.2    Takemoto, Y.3
  • 143
    • 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.-C4
  • 144
    • 17044380275 scopus 로고    scopus 로고
    • Protonated chiral catalysts: Versatile tools for asymmetric synthesis
    • Bolm, C.; Rantanen, T.; Schiffers, I.; Zani, L. Protonated chiral catalysts: Versatile tools for asymmetric synthesis. Angew. Chem. Int. Ed. 2005, 44, 1758-1763.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 1758-1763
    • Bolm, C.1    Rantanen, T.2    Schiffers, I.3    Zani, L.4
  • 145
    • 33746272976 scopus 로고    scopus 로고
    • Chiral phosphoric acids: Powerful organocatalysts for asymmetric addition reactions to imines
    • Connon, S. J. Chiral phosphoric acids: Powerful organocatalysts for asymmetric addition reactions to imines. Angew. Chem. Int. Ed. 2006, 45, 3909-3912.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3909-3912
    • Connon, S.J.1
  • 146
    • 2342521907 scopus 로고    scopus 로고
    • Chiral Brønsted acid-catalyzed direct Mannich reactions via electrophilic activation
    • Uraguchi, D.; Terada, M. Chiral Brønsted acid-catalyzed direct Mannich reactions via electrophilic activation. J. Am. Chem. Soc. 2004, 126, 5356-5357.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5356-5357
    • Uraguchi, D.1    Terada, M.2
  • 147
    • 2342570203 scopus 로고    scopus 로고
    • Enantioselective Mannichtype reaction catalyzed by a chiral Brønsted acid
    • Akiyama, T.; Itoh, J.; Yokota, K.; Fuchibe, K. Enantioselective Mannichtype reaction catalyzed by a chiral Brønsted acid. Angew. Chem. Int. Ed. 2004, 43, 1566-1568.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 1566-1568
    • Akiyama, T.1    Itoh, J.2    Yokota, K.3    Fuchibe, K.4
  • 148
    • 84962407641 scopus 로고    scopus 로고
    • Chiral Brønsted acid catalyzed enantioselective Mannich-type reaction
    • Yamanaka, M.; Itoh, J.; Fuchibe, K.; Akiyama, T. Chiral Brønsted acid catalyzed enantioselective Mannich-type reaction. J. Am. Chem. Soc. 2007, 129, 6756-6764.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 6756-6764
    • Yamanaka, M.1    Itoh, J.2    Fuchibe, K.3    Akiyama, T.4
  • 149
    • 57749118858 scopus 로고    scopus 로고
    • Brønsted acid-catalyzed enantioselective, vinylogous Mannich reaction of vinylketene silyl N,O-acetals
    • Giera, D. S.; Sickert, M.; Schneider, C. Brønsted acid-catalyzed enantioselective, vinylogous Mannich reaction of vinylketene silyl N,O-acetals. Org. Lett. 2008, 10, 4259-4262.
    • (2008) Org. Lett. , vol.10 , pp. 4259-4262
    • Giera, D.S.1    Sickert, M.2    Schneider, C.3
  • 150
    • 33746894125 scopus 로고    scopus 로고
    • Design of Brønsted acid-assisted chiral Brønsted acid catalyst bearing a bis(triflyl)methyl group for a Mannich-type reaction
    • Hasegawa, A.; Naganawa, Y.; Fushimi, M.; Ishihara, K.; Yamamoto, H. Design of Brønsted acid-assisted chiral Brønsted acid catalyst bearing a bis(triflyl)methyl group for a Mannich-type reaction. Org. Lett. 2006, 8, 3175-3178.
    • (2006) Org. Lett. , vol.8 , pp. 3175-3178
    • Hasegawa, A.1    Naganawa, Y.2    Fushimi, M.3    Ishihara, K.4    Yamamoto, H.5
  • 151
    • 56249086830 scopus 로고    scopus 로고
    • Direct organocatalytic Mannich reaction of acetaldehyde: An improved catalyst and mechanistic insight from a computational study
    • Hayashi, H.; Okano, T.; Itoh, T.; Urushima, T.; Ishikawa, H.; Uchimaru, T. Direct organocatalytic Mannich reaction of acetaldehyde: An improved catalyst and mechanistic insight from a computational study. Angew. Chem. Int. Ed. 2008, 47, 9053-9058.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 9053-9058
    • Hayashi, H.1    Okano, T.2    Itoh, T.3    Urushima, T.4    Ishikawa, H.5    Uchimaru, T.6
  • 152
    • 1642369984 scopus 로고    scopus 로고
    • Chiral proton catalysis: A catalytic enantioselective direct aza-Henry reaction
    • Nugent, B. M.; Yoder, R. A.; Johnston, J. N. Chiral proton catalysis: A catalytic enantioselective direct aza-Henry reaction. J. Am. Chem. Soc. 2004, 126, 3418-3419.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 3418-3419
    • Nugent, B.M.1    Yoder, R.A.2    Johnston, J.N.3
  • 153
    • 24044538628 scopus 로고    scopus 로고
    • Chiral Brønsted acid catalyzed enantioselective hydrophosphonylation of imines: symmetric Synthesis of α-amino Phosphonates
    • Akiyama, T.; Morita, H.; Itoh, J.; Fuchibe K. Chiral Brønsted acid catalyzed enantioselective hydrophosphonylation of imines: Asymmetric synthesis of α-amino phosphonates. Org. Lett. 2005, 7, 2583-2585.
    • (2005) A. Org. Lett. , vol.7 , pp. 2583-2585
    • Akiyama, T.1    Morita, H.2    Itoh, J.3    Fuchibe, K.4
  • 154
    • 66449084450 scopus 로고    scopus 로고
    • study on bifunctional chiral Brønsted acidcatalyzed asymmetric hydrophosphonylation of imines
    • Yamanaka, M.; Hirata, T. DFT study on bifunctional chiral Brønsted acidcatalyzed asymmetric hydrophosphonylation of imines. J. Org. Chem. 2009, 74, 3266-3271.
    • (2009) J. Org. Chem. , vol.74 , pp. 3266-3271
    • Yamanaka, M.1    Hirata, T.D.F.T.2
  • 155
    • 33646559779 scopus 로고    scopus 로고
    • A highly enantioselective Brønsted acid catalyst for the Strecker reaction
    • Rueping, M.; Sugiono, E.; Azap, C. A highly enantioselective Brønsted acid catalyst for the Strecker reaction. Angew. Chem. Int. Ed. 2006, 45, 2617-2619.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 2617-2619
    • Rueping, M.1    Sugiono, E.2    Azap, C.3
  • 156
    • 67749103830 scopus 로고    scopus 로고
    • Mechanism of BINOL-phsophoric acidcatalyzed Strecker reaction of benzyl imines
    • Simon, L.; Goodman, J. M. Mechanism of BINOL-phsophoric acidcatalyzed Strecker reaction of benzyl imines. J. Am. Chem. Soc. 2009, 131, 4070-4077.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 4070-4077
    • Simon, L.1    Goodman, J.M.2
  • 157
    • 28044438742 scopus 로고    scopus 로고
    • A powerful Brønsted acid catalyst for the organocatalytic asymmetric transfer hydrogenation of imines
    • Hoffmann, S.; Seayad, A. M.; List, B. A powerful Brønsted acid catalyst for the organocatalytic asymmetric transfer hydrogenation of imines. Angew. Chem. Int. Ed. 2005, 44, 7424-7427.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 7424-7427
    • Hoffmann, S.1    Seayad, A.M.2    List, B.3
  • 158
    • 24044465512 scopus 로고    scopus 로고
    • Enantioselective Brønsted acid catalyzed transfer hydrogenation: Organocatalytic reduction of imines
    • Rueping, M.; Sugiono, E.; Azap, C.; Theissmann, T.; Bolte, M. Enantioselective Brønsted acid catalyzed transfer hydrogenation: Organocatalytic reduction of imines. Org. Lett. 2005, 7, 3781-3783.
    • (2005) Org. Lett. , vol.7 , pp. 3781-3783
    • Rueping, M.1    Sugiono, E.2    Azap, C.3    Theissmann, T.4    Bolte, M.5
  • 159
    • 33646574664 scopus 로고    scopus 로고
    • Metal-free Brønsted acid catalyzed transfer hydrogenation. New organocatalytic reduction of quinolines
    • Rueping, M.; Theissmann, T.; Antonchick, A. P. Metal-free Brønsted acid catalyzed transfer hydrogenation. New organocatalytic reduction of quinolines. Synlett 2006, 1071-1074.
    • (2006) Synlett , pp. 1071-1074
    • Rueping, M.1    Theissmann, T.2    Antonchick, A.P.3
  • 160
    • 33746269442 scopus 로고    scopus 로고
    • A highly enantioselective Brønsted acid catalyzed cascade reaction: Organocatalytic transfer hydrogenation of quinolines and their application in the synthesis of alkaloids
    • Rueping, Antonchick. A. P.; Theissmann, T. A highly enantioselective Brønsted acid catalyzed cascade reaction: Organocatalytic transfer hydrogenation of quinolines and their application in the synthesis of alkaloids. Angew. Chem. Int. Ed. 2006, 45, 3683-3686.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3683-3686
    • Rueping Antonchick, A.P.1    Theissmann, T.2
  • 161
    • 46949083787 scopus 로고    scopus 로고
    • Theoretical study on the mechanism of Hantzsch ester hydrogenation of imines catalyzed by chiral BINOL-phsophoric acids
    • Simon, L.; Goodman, J. M. Theoretical study on the mechanism of Hantzsch ester hydrogenation of imines catalyzed by chiral BINOL-phsophoric acids. J. Am. Chem. Soc. 2008, 130, 8741-8747.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 8741-8747
    • Simon, L.1    Goodman, J.M.2
  • 162
    • 53849122697 scopus 로고    scopus 로고
    • Phosphoric acid catalyzed enantioselective transfer hydrogenation of imines: A density functional theory study of reaction mechanism and the origins of enantioselectivity
    • Marcelli, T.; Hammar, P.; Himo, F. Phosphoric acid catalyzed enantioselective transfer hydrogenation of imines: A density functional theory study of reaction mechanism and the origins of enantioselectivity. Chem. Eur. J. 2008, 14, 8562-8571.
    • (2008) Chem. Eur. J. , vol.14 , pp. 8562-8571
    • Marcelli, T.1    Hammar, P.2    Himo, F.3
  • 163
    • 34250765230 scopus 로고    scopus 로고
    • Organocatalytic enantioselective reduction of pyridines
    • Rueping, M.; Antonchick, A. P. Organocatalytic enantioselective reduction of pyridines. Angew. Chem. Int. Ed. 2007, 46, 4562-4565.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 4562-4565
    • Rueping, M.1    Antonchick, A.P.2
  • 165
    • 33749534513 scopus 로고    scopus 로고
    • Catalytic asymmetric reductive amination of aldehydes via dynamic kinetic resolution
    • Hoffmann, S.; Nicoletti, M.; List, B. Catalytic asymmetric reductive amination of aldehydes via dynamic kinetic resolution. J. Am. Chem. Soc. 2006, 128, 13074-13075.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 13074-13075
    • Hoffmann, S.1    Nicoletti, M.2    List, B.3
  • 166
    • 4644355914 scopus 로고    scopus 로고
    • Organocatalytic asymmetric aza- Friedel-Crafts alkylation of furan
    • Uraguchi, D.; Sorimachi, K.; Terada, M. Organocatalytic asymmetric aza- Friedel-Crafts alkylation of furan. J. Am. Chem. Soc. 2004, 126, 11804-11805.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 11804-11805
    • Uraguchi, D.1    Sorimachi, K.2    Terada, M.3
  • 167
    • 67649344302 scopus 로고    scopus 로고
    • Organocatalytic enantioselective aza-Friedel-Crafts alkylation of pyrroles with N- (heteroarenesulfonyl)imines
    • Nakamura S.; Sakurai, Y.; Nakashima, H.; Shibata, N.; Toru, T. Organocatalytic enantioselective aza-Friedel-Crafts alkylation of pyrroles with N- (heteroarenesulfonyl)imines. Synlett 2009, 1639-1642.
    • (2009) Synlett , pp. 1639-1642
    • Nakamura, S.1    Sakurai, Y.2    Nakashima, H.3    Shibata, N.4    Toru, T.5
  • 168
    • 53849146708 scopus 로고    scopus 로고
    • Chiral Brønsted acid-mediated enantioselective organocatalytic three component reaction for the construction of trifluoromethyl-containing molecules
    • Zhang, G.-W.; Wang, L.; Nie, J.; Ma, J.A. Chiral Brønsted acid-mediated enantioselective organocatalytic three component reaction for the construction of trifluoromethyl-containing molecules. Adv. Synth. Catal. 2008, 350, 1457-1463.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 1457-1463
    • Zhang, G.-W.1    Wang, L.2    Nie, J.3    Ma, J.A.4
  • 169
    • 31944452587 scopus 로고    scopus 로고
    • Catalytic asymmetric Pictet-Spengler reaction
    • Seayad, J.; Seayad, A. M.; List, B. Catalytic asymmetric Pictet-Spengler reaction. J. Am. Chem. Soc. 2006, 128, 1086-1087.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 1086-1087
    • Seayad, J.1    Seayad, A.M.2    List, B.3
  • 170
    • 85196433463 scopus 로고    scopus 로고
    • For a review on organocatalytic Diels-Alder reactions see
    • For a review on organocatalytic Diels-Alder reactions see
  • 172
    • 33846157409 scopus 로고    scopus 로고
    • Enantioselective direct aza hetero-Diels-Alder reaction catalyzed by chiral Brønsted acids
    • Liu, H.; Cun, L.-F.; Mi, A-Q.; Jiang, Y.-Z.; Gong, L.-Z. Enantioselective direct aza hetero-Diels-Alder reaction catalyzed by chiral Brønsted acids. Org. Lett. 2006, 8, 6023-6026.
    • (2006) Org. Lett. , vol.8 , pp. 6023-6026
    • Liu, H.1    Cun, L.-F.2    Mi, A.-Q.3    Jiang, Y.-Z.4    Gong, L.-Z.5
  • 173
    • 33845329553 scopus 로고    scopus 로고
    • Cooperative coexistence: Effective interplay of two Brønsted acids in the asymmetric synthesis of isoquinuclidines
    • Rueping, M.; Azap, C. Cooperative coexistence: effective interplay of two Brønsted acids in the asymmetric synthesis of isoquinuclidines. Angew. Chem. Int. Ed. 2006, 45, 7832-7835.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 7832-7835
    • Rueping, M.1    Azap, C.2
  • 174
    • 33749522044 scopus 로고    scopus 로고
    • Chiral Brønsted acid-catalyzed inverse electron-demand aza-Diels-Alder reaction
    • Akiyama, T.; Morita, H.; Fuchibe, K. Chiral Brønsted acid-catalyzed inverse electron-demand aza-Diels-Alder reaction. J. Am. Chem. Soc. 2006, 128, 13070-13071.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 13070-13071
    • Akiyama, T.1    Morita, H.2    Fuchibe, K.3
  • 175
    • 33746292951 scopus 로고    scopus 로고
    • High substrate/catalyst organocatalysis by a chiral Brønsted acid for an enantioselective aza-ene-type reaction
    • Terada, M.; Machioka, K.; Sorimachi, K. High substrate/catalyst organocatalysis by a chiral Brønsted acid for an enantioselective aza-ene-type reaction. Angew. Chem. Int. Ed. 2006, 45, 2254-2257.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 2254-2257
    • Terada, M.1    Machioka, K.2    Sorimachi, K.3
  • 176
    • 21644449826 scopus 로고    scopus 로고
    • Organocatalytic asymmetric direct alkylation of α-diazoester via C-H bond cleavage
    • Uraguchi, D.; Sorimachi, K.; Terada, M. Organocatalytic asymmetric direct alkylation of α-diazoester via C-H bond cleavage. J. Am. Chem. Soc. 2005, 127, 9360-9361.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 9360-9361
    • Uraguchi, D.1    Sorimachi, K.2    Terada, M.3
  • 179
    • 53249085441 scopus 로고    scopus 로고
    • nantioselective 1,3-dipolar cycloaddition of nitrones with ethyl vinyl ether: The difference between Brønsted catalysis and Lewis acid catalysis
    • Jiao, P.; Nakashima, D.; Yamamoto, H. Enantioselective 1,3-dipolar cycloaddition of nitrones with ethyl vinyl ether: The difference between Brønsted catalysis 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
  • 180
    • 33845205051 scopus 로고    scopus 로고
    • Highly enantioselective organocatalytic Bignelli reaction
    • Chen, X.-H.; Xu, X.-Y.; Liu, H.; Cun, L.-F.; Gong, L.-Z. Highly enantioselective organocatalytic Bignelli reaction. J. Am. Chem. Soc. 2006, 128, 14802-14803.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 14802-14803
    • Chen, X.-H.1    Xu, X.-Y.2    Liu, H.3    Cun, L.-F.4    Gong, L.-Z.5
  • 181
    • 70350307205 scopus 로고    scopus 로고
    • Highly enantioselective organocatalytic Biginelli and Biginelli-like condensations: Reversal of the stereochemistry by tuning the 3,3'-disubstituents of phosphoric acids
    • Li, N.; Chen, X.-H.; Song, J.; Luo, S.-W.; Fan, W.; Gong, L.-Z. Highly enantioselective organocatalytic Biginelli and Biginelli-like condensations: Reversal of the stereochemistry by tuning the 3,3'-disubstituents of phosphoric acids. J. Am. Chem. Soc. 2009, 131, 15301-15310.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 15301-15310
    • Li, N.1    Chen, X.-H.2    Song, J.3    Luo, S.-W.4    Fan, W.5    Gong, L.-Z.6


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