메뉴 건너뛰기




Volumn 16, Issue 20, 2012, Pages 2440-2461

Bifunctional organocatalysts in the asymmetric michael additions of carbonylic compounds to nitroalkenes

Author keywords

Asymmetric; Bifunctional; Ketones; Michael Additions; Nitroalkenes; Organocatalysts

Indexed keywords

ADDITION REACTIONS; CARBON; COVALENT BONDS; KETONES; STEREOCHEMISTRY; SULFUR COMPOUNDS;

EID: 84872579652     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527212803520128     Document Type: Article
Times cited : (46)

References (128)
  • 1
    • 0036089366 scopus 로고    scopus 로고
    • Asymmetric Michael additions to nitroalkenes
    • Berner, O.M.; Tedeschi, L.; Enders, D. Asymmetric Michael additions to nitroalkenes. Eur. J. Org. Chem., 2002, (12), 1877-1894.
    • (2002) Eur. J. Org. Chem , Issue.12 , pp. 1877-1894
    • Berner, O.M.1    Tedeschi, L.2    Enders, D.3
  • 2
    • 0842322178 scopus 로고    scopus 로고
    • Catalytic, enantioselective Michael addition reactions
    • Jha, S.C.; Joshi, N.N. Catalytic, enantioselective Michael addition reactions. ARKIVOC, 2002, (vii), 167-196.
    • (2002) ARKIVOC , Issue.8 , pp. 167-196
    • Jha, S.C.1    Joshi, N.N.2
  • 3
    • 0035126119 scopus 로고    scopus 로고
    • Recent advances in catalytic enantioselective Michael additions
    • Krause, N.; Hoffmann-Roder, A. Recent advances in catalytic enantioselective Michael additions. Synthesis, 2001, (2), 171-196.
    • (2001) Synthesis , Issue.2 , pp. 171-196
    • Krause, N.1    Hoffmann-Roder, A.2
  • 4
    • 7044235263 scopus 로고    scopus 로고
    • Domino reactions in organic synthesis
    • Tietze, L.F. Domino reactions in organic synthesis. Chem. Rev., 1996, 96(1), 115-136.
    • (1996) Chem. Rev , vol.96 , Issue.1 , pp. 115-136
    • Tietze, L.F.1
  • 5
    • 0028879573 scopus 로고
    • Recent advances in the use of tandem reactions for organic synthesis
    • Bunce, R.A. Recent advances in the use of tandem reactions for organic synthesis. Tetrahedron, 1995, 51(48), 13103-13159.
    • (1995) Tetrahedron , vol.51 , Issue.48 , pp. 13103-13159
    • Bunce, R.A.1
  • 6
    • 57049084768 scopus 로고    scopus 로고
    • Synthesis of highly substituted pyroglutamates via a domino Michael addition-Claisen rearrangement-lactamisation approach
    • Schmidt, C.; Kazamaier, U. Synthesis of highly substituted pyroglutamates via a domino Michael addition-Claisen rearrangement-lactamisation approach. Org. Biomol. Chem., 2008, 6, 4643-4648.
    • (2008) Org. Biomol. Chem , vol.6 , pp. 4643-4648
    • Schmidt, C.1    Kazamaier, U.2
  • 7
    • 80052833054 scopus 로고    scopus 로고
    • Enantioselective Michael/cyclization reaction sequence: Scaffold-inspired synthesis of spirooxindoles with multiple stereocenters
    • Cao, Y.; Jiang, X.; Liu, L.; Shen, F.; Zhang, F.; Wang, R. Enantioselective Michael/cyclization reaction sequence: scaffold-inspired synthesis of spirooxindoles with multiple stereocenters. Angew. Chem. Int. Ed., 2011, 50(39) 9124-9127.
    • (2011) Angew. Chem. Int. Ed , vol.50 , Issue.39 , pp. 9124-9127
    • Cao, Y.1    Jiang, X.2    Liu, L.3    Shen, F.4    Zhang, F.5    Wang, R.6
  • 8
    • 78650383618 scopus 로고    scopus 로고
    • Catalytic asymmetric domino Michael addition-alkylation reaction: Enantioselective synthesis of dihydrofurans
    • Rueping, M.; Parra, A; Uria, U.; Besselièvre, F; Meerino, E. Catalytic asymmetric domino Michael addition-alkylation reaction: enantioselective synthesis of dihydrofurans. Org. Lett., 2010, 12(24), 5680-5683.
    • (2010) Org. Lett , vol.12 , Issue.24 , pp. 5680-5683
    • Rueping, M.1    Parra, A.2    Uria, U.3    Besselièvre, F.4    Meerino, E.5
  • 9
    • 0036625219 scopus 로고    scopus 로고
    • Lanthanide complexes in multifunctional asymmetric catalysis
    • Shibasaki, M.; Yoshikawa, N. Lanthanide complexes in multifunctional asymmetric catalysis. Chem. Rev., 2002, 102(6), 2187-2210.
    • (2002) Chem. Rev , vol.102 , Issue.6 , pp. 2187-2210
    • Shibasaki, M.1    Yoshikawa, N.2
  • 10
    • 33645681534 scopus 로고    scopus 로고
    • Bifunctional transition metal-based molecular catalysts for asymmetric syntheses
    • Ikariya, T.; Murata, K.; Noyori, R. Bifunctional transition metal-based molecular catalysts for asymmetric syntheses. Org. Biomol. Chem., 2006, 4, 393-406.
    • (2006) Org. Biomol. Chem , vol.4 , pp. 393-406
    • Ikariya, T.1    Murata, K.2    Noyori, R.3
  • 11
    • 34547623607 scopus 로고    scopus 로고
    • Asymmetric organocatalysis
    • Pellissier, H. Asymmetric organocatalysis. Tetrahedron, 2007, 63(38), 9267-9331.
    • (2007) Tetrahedron , vol.63 , Issue.38 , pp. 9267-9331
    • Pellissier, H.1
  • 12
    • 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(12), 5713-5743.
    • (2007) Chem. Rev , vol.107 , Issue.12 , pp. 5713-5743
    • Doyle, A.G.1    Jacobsen, E.N.2
  • 13
    • 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(5), 289-296.
    • (2003) Chem. Soc. Rev , vol.32 , Issue.5 , pp. 289-296
    • Schreiner, P.R.1
  • 14
    • 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(9), 999-1010.
    • (2006) Adv. Synth. Catal , vol.348 , Issue.9 , pp. 999-1010
    • Akiyama, T.1    Itoh, J.2    Fuchibe, K.3
  • 15
    • 33746277515 scopus 로고    scopus 로고
    • Organocatalysis mediated by (thio)urea derivatives
    • Connon, S. J. Organocatalysis mediated by (thio)urea derivatives. Chem. A Eur. J., 2006, 12(21), 5418-5427.
    • (2006) Chem. A Eur. J , vol.12 , Issue.21 , pp. 5418-5427
    • Connon, S.J.1
  • 16
    • 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
  • 17
    • 70349617279 scopus 로고    scopus 로고
    • Bifunctional chiral organocatalysts in organic transformations. Curr
    • Bhadury, P.S.; Song, B.-A.; Yang, S.; Hu, D.-Y.; Xue, W. Bifunctional chiral organocatalysts in organic transformations. Curr. Org. Synth., 2009, 6(4), 380-399.
    • (2009) Org. Synth , vol.6 , Issue.4 , pp. 380-399
    • Bhadury, P.S.1    Song, B.-A.2    Yang, S.3    Hu, D.-Y.4    Xue, W.5
  • 20
    • 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
  • 21
    • 80054740926 scopus 로고    scopus 로고
    • Enantioselective phospha-Michael reaction of diphenyl phosphonate with nitroolefins utilizing conformationally flexible guanidinium/bisthiourea organocatalyst: Assembly-state tunability in asymmetric organocatalysis
    • Sohtome, Y.; Horitsugi, N.; Takagi, R.; Nagasawa, K. Enantioselective phospha-Michael reaction of diphenyl phosphonate with nitroolefins utilizing conformationally flexible guanidinium/bisthiourea organocatalyst: assembly-state tunability in asymmetric organocatalysis. Adv. Synth. Catal., 2011, 353(14-15), 2631-2636.
    • (2011) Adv. Synth. Catal , vol.353 , Issue.14-15 , pp. 2631-2636
    • Sohtome, Y.1    Horitsugi, N.2    Takagi, R.3    Nagasawa, K.4
  • 23
    • 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(4), 1187-1198.
    • (2009) Chem. Soc. Rev , vol.38 , Issue.4 , pp. 1187-1198
    • Zhang, Z.1    Schreiner, P.R.2
  • 24
    • 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(10), 1520-1543.
    • (2006) Angew. Chem. Int. Ed , vol.45 , Issue.10 , pp. 1520-1543
    • Taylor, M.S.1    Jacobsen, E.N.2
  • 25
    • 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 (8), 580-591.
    • (2004) Acc. Chem. Res , vol.37 , Issue.8 , pp. 580-591
    • Notz, W.1    Tanaka, F.2    Barbas III, C.F.3
  • 26
    • 0000761777 scopus 로고    scopus 로고
    • Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins
    • List, B.; Pojaliev, P.; Martin, H.J. Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins. Org. Lett., 2001, 3(16), 2423-2425.
    • (2001) Org. Lett , vol.3 , Issue.16 , pp. 2423-2425
    • List, B.1    Pojaliev, P.2    Martin, H.J.3
  • 27
    • 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(8), 548-557.
    • (2004) Acc. Chem. Res , vol.37 , Issue.8 , pp. 548-557
    • List, B.1
  • 28
    • 34547158079 scopus 로고    scopus 로고
    • 4,4'-disubstituted-L-proline catalyzes the direct asymmetric Michael addition of aldehydes to nitrostyrenes
    • Gu, L.-Q.; Zhao, G. 4,4'-disubstituted-L-proline catalyzes the direct asymmetric Michael addition of aldehydes to nitrostyrenes. Adv. Synth. Catal., 2007, 349, 1629-1632.
    • (2007) Adv. Synth. Catal , vol.349 , pp. 1629-1632
    • Gu, L.-Q.1    Zhao, G.2
  • 29
    • 33748791724 scopus 로고    scopus 로고
    • Highly efficient asymmetric Michael addition of aldehydes to nitroalkenes catalyzed by a simple trans-4-hydroxyprolylamide
    • Palomo, C.; Vera, S.; Mielgo, A.; Gómez-Bengoa, E. Highly efficient asymmetric Michael addition of aldehydes to nitroalkenes catalyzed by a simple trans-4-hydroxyprolylamide. Angew. Chem. Int. Ed., 2006, 45(36), 5984-5987.
    • (2006) Angew. Chem. Int. Ed , vol.45 , Issue.36 , pp. 5984-5987
    • Palomo, C.1    Vera, S.2    Mielgo, A.3    Gómez-Bengoa, E.4
  • 30
    • 26044455689 scopus 로고    scopus 로고
    • Highly enantioselective (S)-homoproline-catalyzed Michael addition reactions of ketones to β-nitrostyrenes
    • Terakado, D.; Takano, M.; Oriyama, T. Highly enantioselective (S)-homoproline-catalyzed Michael addition reactions of ketones to β-nitrostyrenes. Chem. Lett., 2005, 34(7), 962-963.
    • (2005) Chem. Lett , vol.34 , Issue.7 , pp. 962-963
    • Terakado, D.1    Takano, M.2    Oriyama, T.3
  • 31
    • 79953231242 scopus 로고    scopus 로고
    • (S)-Binam-L-prolinamide as organocatalyst for the enantioselective conjugate addition of α-alkoxyketones to β-nitrostyrene derivatives
    • Guillena, G.; Nájera, C.; Viózquez, S.F.; Yus, M. (S)-Binam-L-prolinamide as organocatalyst for the enantioselective conjugate addition of α-alkoxyketones to β-nitrostyrene derivatives. ARKIVOC, 2011, 111, 166-178.
    • (2011) ARKIVOC , vol.111 , pp. 166-178
    • Guillena, G.1    Nájera, C.2    Viózquez, S.F.3    Yus, M.4
  • 32
    • 33747758648 scopus 로고    scopus 로고
    • Enantioselective conjugate addition of ketones to β-nitrostyrenes catalyzed by 1,2-amino alcohol-derived prolinamides
    • Almaşi, D.; Alonso, D.A.; Nájera, C. Enantioselective conjugate addition of ketones to β-nitrostyrenes catalyzed by 1,2-amino alcohol-derived prolinamides. Tetrahedron: Asymmetry, 2006, 17, 2064-2068.
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 2064-2068
    • Almaşi, D.1    Alonso, D.A.2    Nájera, C.3
  • 33
    • 70349292429 scopus 로고    scopus 로고
    • Novel prolinamidecamphor-containing organocatalysts for direct asymmetric Michael addition of unmodified aldehydes to nitroalkenes
    • Reddy, R.J.; Kuan, H.-H.; Chou, T.-Y.; Chen, K. Novel prolinamidecamphor-containing organocatalysts for direct asymmetric Michael addition of unmodified aldehydes to nitroalkenes. Chem. Eur. J., 2009, 15, 9294-9298.
    • (2009) Chem. Eur. J , vol.15 , pp. 9294-9298
    • Reddy, R.J.1    Kuan, H.-H.2    Chou, T.-Y.3    Chen, K.4
  • 35
    • 74849117325 scopus 로고    scopus 로고
    • Enamine catalysis with low catalyst loadings-high efficiency via kinetic studies
    • Wiesner, M.; Upert, G.; Angelici, G.; Wennemers, H. Enamine catalysis with low catalyst loadings-high efficiency via kinetic studies. J. Am. Chem. Soc., 2010, 132, 6-7.
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 6-7
    • Wiesner, M.1    Upert, G.2    Angelici, G.3    Wennemers, H.4
  • 36
    • 70349675488 scopus 로고    scopus 로고
    • 2as catalysts for asymmetric 1,4-addition reactions: Structural requirements for high catalytic efficiency
    • 2as catalysts for asymmetric 1,4-addition reactions: structural requirements for high catalytic efficiency. Chem. Eur. J., 2009, 15, 10103-10109.
    • (2009) Chem. Eur. J , vol.15 , pp. 10103-10109
    • Wiesner, M.1    Neuburger, M.2    Wennemers, H.3
  • 37
    • 80052703436 scopus 로고    scopus 로고
    • Proline-based reduced dipeptides as recyclable and highly enantioselective organocatalyst for asymmetric Michael addition
    • Cao, X.; Wang, G.; Zhang, R.; Wei, Y.; Wang, W.; Sun, H.; Chen, L. Proline-based reduced dipeptides as recyclable and highly enantioselective organocatalyst for asymmetric Michael addition. Org. Biomol. Chem., 2011, 9, 6487-6490.
    • (2011) Org. Biomol. Chem , vol.9 , pp. 6487-6490
    • Cao, X.1    Wang, G.2    Zhang, R.3    Wei, Y.4    Wang, W.5    Sun, H.6    Chen, L.7
  • 38
    • 33645909878 scopus 로고    scopus 로고
    • Small peptidecatalyzed enantioselective addition of ketones to nitroolefins
    • Xu, Y.; Zou, W.; Sundén, H.; Ibrahem, I.; Córdova, A. Small peptidecatalyzed enantioselective addition of ketones to nitroolefins. Adv. Synth. Catal., 2006, 348, 418-424.
    • (2006) Adv. Synth. Catal , vol.348 , pp. 418-424
    • Xu, Y.1    Zou, W.2    Sundén, H.3    Ibrahem, I.4    Córdova, A.5
  • 39
    • 33645035954 scopus 로고    scopus 로고
    • Simple highly modular acyclic amine-catalyzed direct enantioselective addition of ketones to nitro-olefins
    • Xu, Y.; Córdova, A. Simple highly modular acyclic amine-catalyzed direct enantioselective addition of ketones to nitro-olefins. Chem. Commun., 2006, 460-462.
    • (2006) Chem. Commun , pp. 460-462
    • Xu, Y.1    Córdova, A.2
  • 40
    • 80052756991 scopus 로고    scopus 로고
    • β-Amino acid catalyzed asymmetric Michael addition: Design of organocatalysts with catalytic acid/base dyad inspired by serine proteases
    • Yang, H.; Wong, M.W. β-Amino acid catalyzed asymmetric Michael addition: design of organocatalysts with catalytic acid/base dyad inspired by serine proteases. J. Org. Chem., 2011, 76, 7399-7405.
    • (2011) J. Org. Chem , vol.76 , pp. 7399-7405
    • Yang, H.1    Wong, M.W.2
  • 41
    • 4043184288 scopus 로고    scopus 로고
    • Direct asymmetric organocatalytic Michael reactions of α, α-disubstituted aldehydes with β-nitrostyrenes for the synthesis of quaternary carbon-containing products
    • Mase, N.; Thayumanavan, R.; Tanaka, F.; Barbas III, C.F. Direct asymmetric organocatalytic Michael reactions of α, α-disubstituted aldehydes with β-nitrostyrenes for the synthesis of quaternary carbon-containing products. Org. Lett., 2004, 6(15). 2527-2530.
    • (2004) Org. Lett , vol.6 , Issue.15 , pp. 2527-2530
    • Mase, N.1    Thayumanavan, R.2    Tanaka, F.3    Barbas III, C.F.4
  • 42
    • 0035796953 scopus 로고    scopus 로고
    • Catalytic enantioselective direct Michael additions of ketones to alkylidene malonates
    • Betancort, J.M.; Sakthivel, K.; Thayumanavan, R.; Barbas III, C.F. Catalytic enantioselective direct Michael additions of ketones to alkylidene malonates. Tetrahedron Lett., 2001, 42, 4441-4444.
    • (2001) Tetrahedron Lett , vol.42 , pp. 4441-4444
    • Betancort, J.M.1    Sakthivel, K.2    Thayumanavan, R.3    Barbas III, C.F.4
  • 43
    • 0035891780 scopus 로고    scopus 로고
    • Catalytic direct asymmetric Michael reactions: Taming naked aldehyde donors
    • Betancort, J.M.; Barbas III, C.F. Catalytic direct asymmetric Michael reactions: taming naked aldehyde donors. Org. Lett., 2001, 3(23), 3737-3740.
    • (2001) Org. Lett , vol.3 , Issue.23 , pp. 3737-3740
    • Betancort, J.M.1    Barbas III, C.F.2
  • 44
    • 33646142092 scopus 로고    scopus 로고
    • Organocataytic direct Michael reaction of ketones and aldehydes with β-nitrostyrene in brine
    • Mase, N., Watanabe, K.; Yoda, H.; Takabe, K.; Tanaka, F.; Barbas III, C.F. Organocataytic direct Michael reaction of ketones and aldehydes with β-nitrostyrene in brine. J. Am. Chem. Soc. 2006, 128, 4966-4967.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 4966-4967
    • Mase, N.1    Watanabe, K.2    Yoda, H.3    Takabe, K.4    Tanaka, F.5    Barbas III, C.F.6
  • 46
    • 3543065878 scopus 로고    scopus 로고
    • A new class of chiral pyrrolidine-pyridine conjugate base catalysts for use in asymmetric Michael addition reactions
    • Ishii, T.; Fujioka, S.; Sekiguchi, Y.; Kotsuki, H. A new class of chiral pyrrolidine-pyridine conjugate base catalysts for use in asymmetric Michael addition reactions. J. Am. Chem. Soc., 2004, 126, 9558-9859.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 9558-9859
    • Ishii, T.1    Fujioka, S.2    Sekiguchi, Y.3    Kotsuki, H.4
  • 47
    • 77956709763 scopus 로고    scopus 로고
    • A novel chiral aliphatic-aromatic diamine promoted direct, highly enantio-and diasteroselective Michael addition of cyclohexanone to nitroolefins under solvent-free conditions
    • Miao, S.; Bai, J.; Yang, J.; Zhang, Y. A novel chiral aliphatic-aromatic diamine promoted direct, highly enantio-and diasteroselective Michael addition of cyclohexanone to nitroolefins under solvent-free conditions. Chirality, 2010, 22, 855-862.
    • (2010) Chirality , vol.22 , pp. 855-862
    • Miao, S.1    Bai, J.2    Yang, J.3    Zhang, Y.4
  • 48
    • 33746596576 scopus 로고    scopus 로고
    • Simple diamine-and triamine-protonic acid catalyst for the enantioselective Michael addition of cyclic ketones to nitroalkenes
    • Pansare, S.V.; Pandya, K. Simple diamine-and triamine-protonic acid catalyst for the enantioselective Michael addition of cyclic ketones to nitroalkenes J. Am. Chem. Soc., 2006, 128, 9624-9625.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 9624-9625
    • Pansare, S.V.1    Pandya, K.2
  • 49
    • 33645884137 scopus 로고    scopus 로고
    • A highly enantioselective organocatalyst for the Michael addition of cyclic ketones to nitroolefins
    • Zhu, M.-K.; Cun, L.-F.; Mi, A.-Q.; Jiang, Y.-Z.; Gong, L.-Z. A highly enantioselective organocatalyst for the Michael addition of cyclic ketones to nitroolefins. Tetrahedron: Asymmetry, 2006, 17, 491-493.
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 491-493
    • Zhu, M.-K.1    Cun, L.-F.2    Mi, A.-Q.3    Jiang, Y.-Z.4    Gong, L.-Z.5
  • 50
    • 0000220483 scopus 로고    scopus 로고
    • Diamine-catalyzed asymmetric Michael addition of aldehydes and ketones to nitrostyrene
    • Alexakis, A.; Andrey, O. Diamine-catalyzed asymmetric Michael addition of aldehydes and ketones to nitrostyrene. Org. Lett., 2002, 4(21), 3611-3614.
    • (2002) Org. Lett , vol.4 , Issue.21 , pp. 3611-3614
    • Alexakis, A.1    Andrey, O.2
  • 51
    • 0141563562 scopus 로고    scopus 로고
    • Asymmetric Michael addition of α-hydroxyketones to nitroolefins catalyzed by chiral diamine
    • Andrey, O.; Alexakis, A.; Bernardinelli, G. Asymmetric Michael addition of α-hydroxyketones to nitroolefins catalyzed by chiral diamine. Org. Lett., 2003, 5(14), 2559-2561.
    • (2003) Org. Lett , vol.5 , Issue.14 , pp. 2559-2561
    • Andrey, O.1    Alexakis, A.2    Bernardinelli, G.3
  • 52
    • 33745542958 scopus 로고    scopus 로고
    • 3,3'-Bimorpholine derivatives as a new class of organocatalysts for asymmetric Michael addition
    • Mossé, S.; Laars, M.; Kriis, K.; Kanger, T.; Alexakis, A. 3,3'-Bimorpholine derivatives as a new class of organocatalysts for asymmetric Michael addition. Org. Lett., 2006, 8(12), 2559-2562.
    • (2006) Org. Lett , vol.8 , Issue.12 , pp. 2559-2562
    • Mossé, S.1    Laars, M.2    Kriis, K.3    Kanger, T.4    Alexakis, A.5
  • 53
    • 77952666618 scopus 로고    scopus 로고
    • Asymmetric Michael addition of ketones to nitroolefins catalyzed by a new chiral catalyst
    • Wang, L.-J.; Hu, F.-F. Asymmetric Michael addition of ketones to nitroolefins catalyzed by a new chiral catalyst. Bull. Korean Chem. Soc., 2010, 31(5), 1280-1282.
    • (2010) Bull. Korean Chem. Soc , vol.31 , Issue.5 , pp. 1280-1282
    • Wang, L.-J.1    Hu, F.-F.2
  • 54
    • 78751570918 scopus 로고    scopus 로고
    • Pyrrolidine-linkercamphor assembly: Bifunctional organocatalysts for efficient Michael addition of cyclohexanone to nitroolefins under neat conditions
    • Anwar, S.; Lee, P.-H.; Chou, T.-Y.; Chang, C.; Chen, K. Pyrrolidine-linkercamphor assembly: bifunctional organocatalysts for efficient Michael addition of cyclohexanone to nitroolefins under neat conditions. Tetrahedron, 2011, 67, 1171-1177.
    • (2011) Tetrahedron , vol.67 , pp. 1171-1177
    • Anwar, S.1    Lee, P.-H.2    Chou, T.-Y.3    Chang, C.4    Chen, K.5
  • 55
    • 77953563112 scopus 로고    scopus 로고
    • Pyrrolidinylcamphor derivatives as a new class of oraganocatalyst for direct asymmetric Michael addition of aldehydes an ketones to β-nitroalkenes
    • Ting, Y.-F.; Chang, C.; Reddy, R.J.; Magar, D.R.; Chen, K. Pyrrolidinylcamphor derivatives as a new class of oraganocatalyst for direct asymmetric Michael addition of aldehydes an ketones to β-nitroalkenes. Chem. Eur. J. 2010, 16, 7030-7038.
    • (2010) Chem. Eur. J , vol.16 , pp. 7030-7038
    • Ting, Y.-F.1    Chang, C.2    Reddy, R.J.3    Magar, D.R.4    Chen, K.5
  • 56
    • 78649277219 scopus 로고    scopus 로고
    • 3-Symmetric proline-functionlized organocatalyst: Enantioselective Michael addition reactions
    • 3-Symmetric proline-functionlized organocatalyst: enantioselective Michael addition reactions. Eur. J. Org. Chem., 2010, 6359-6365.
    • (2010) Eur. J. Org. Chem , pp. 6359-6365
    • Moorthy, J.N.1    Saha, S.2
  • 58
    • 4644317493 scopus 로고    scopus 로고
    • 5-pyrrolidin-2-yltetrazole as an asymmetric organocatalyst for the addition of ketones to nitro-olefins
    • Cobb, A.J.A.; Longbottom, D.A.; Shaw, D.M.; Ley, S.V. 5-pyrrolidin-2-yltetrazole as an asymmetric organocatalyst for the addition of ketones to nitro-olefins. Chem. Commun., 2004, 1808-1809.
    • (2004) Chem. Commun , pp. 1808-1809
    • Cobb, A.J.A.1    Longbottom, D.A.2    Shaw, D.M.3    Ley, S.V.4
  • 59
    • 77953881545 scopus 로고    scopus 로고
    • Chiral pyrrolidineazole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes
    • Zhang, L.; Xu, H.; Mi, X.-L.; Luo, S.-Z.; Cheng, J.-P. Chiral pyrrolidineazole conjugates: simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes. Chinese Sci. Bull., 2010, 55(17), 1735-1741.
    • (2010) Chinese Sci. Bull , vol.55 , Issue.17 , pp. 1735-1741
    • Zhang, L.1    Xu, H.2    Mi, X.-L.3    Luo, S.-Z.4    Cheng, J.-P.5
  • 60
    • 33751581895 scopus 로고    scopus 로고
    • Evolution of pyrrolidine-type asymmetric organocatalyst by "Click" chemistry
    • Luo, S.; Xu, H.; Mi, X.; Li, J.; Zheng, X.; Cheng, J.-P. Evolution of pyrrolidine-type asymmetric organocatalyst by "Click" chemistry. J. Org. Chem., 2006, 71, 9244-9247.
    • (2006) J. Org. Chem , vol.71 , pp. 9244-9247
    • Luo, S.1    Xu, H.2    Mi, X.3    Li, J.4    Zheng, X.5    Cheng, J.-P.6
  • 61
    • 79956364920 scopus 로고    scopus 로고
    • A chiral pyrrolidine-pyrazole catalyst for the enantioselective Michael addition of carbonyls to nitroolefins
    • Chandrasekhar, S.; Kumar, T.P.; Haribabu, K.; Reddy, C.R.; Kumar, C.R.; A chiral pyrrolidine-pyrazole catalyst for the enantioselective Michael addition of carbonyls to nitroolefins. Tetrahedron:Asymmetry, 2011, 22, 697-702.
    • (2011) Tetrahedron:Asymmetry , vol.22 , pp. 697-702
    • Chandrasekhar, S.1    Kumar, T.P.2    Haribabu, K.3    Reddy, C.R.4    Kumar, C.R.5
  • 62
    • 78149280139 scopus 로고    scopus 로고
    • Hydroxyphthalimide allied triazole-pyrrolidine catalyst for asymmetric Michael addition in water
    • Chandrasekhar, S.; Kumar, T.P.; Haribabu, K.; Reddy, C.R. Hydroxyphthalimide allied triazole-pyrrolidine catalyst for asymmetric Michael addition in water. Tetrahedron:Asymmetry, 2010, 21, 2372-2375.
    • (2010) Tetrahedron:Asymmetry , vol.21 , pp. 2372-2375
    • Chandrasekhar, S.1    Kumar, T.P.2    Haribabu, K.3    Reddy, C.R.4
  • 63
    • 80155125049 scopus 로고    scopus 로고
    • Highly enantioselective Michael addition of ketones to nitroolefins with a pyrrolidine-based phthalimide as an enamine-type organocatlyst
    • Ban, S.R.; Xie, H.-Y.; Zhu, X.-X.; Li, Q.-S. Highly enantioselective Michael addition of ketones to nitroolefins with a pyrrolidine-based phthalimide as an enamine-type organocatlyst. Eur. J. Org. Chem., 2011, 6413-6417.
    • (2011) Eur. J. Org. Chem , pp. 6413-6417
    • Ban, S.R.1    Xie, H.-Y.2    Zhu, X.-X.3    Li, Q.-S.4
  • 64
    • 79954449562 scopus 로고    scopus 로고
    • Novel pyrrolidine-thiohydantoin/thioxotetrahydropyrimidinones as highly effective catalysts for the asymmetric Michael addition
    • Kokotos, C.G.; Limnios, D.; Triggidou, D.; Trifonidou, M.; Kokotos, G. Novel pyrrolidine-thiohydantoin/thioxotetrahydropyrimidinones as highly effective catalysts for the asymmetric Michael addition. Org. Biomol. Chem., 2011, 9, 3386-3395.
    • (2011) Org. Biomol. Chem , vol.9 , pp. 3386-3395
    • Kokotos, C.G.1    Limnios, D.2    Triggidou, D.3    Trifonidou, M.4    Kokotos, G.5
  • 65
    • 77957145723 scopus 로고    scopus 로고
    • Thiazolidine-based organocatalysts for a highly enantioselective direct aldol reaction
    • Rambo, R.S.; Schneider, P.H. Thiazolidine-based organocatalysts for a highly enantioselective direct aldol reaction. Tetrahedron: Asymmetry, 2010, 21(18), 2254-2257.
    • (2010) Tetrahedron: Asymmetry , vol.21 , Issue.18 , pp. 2254-2257
    • Rambo, R.S.1    Schneider, P.H.2
  • 66
    • 78249284338 scopus 로고    scopus 로고
    • Silylated pyrrolidines as catalysts for asymmetric Michael additions of aldehydes to nitroolefins
    • Husmann, R.; Jörres, M.; Raabe, G.; Bolm, C. Silylated pyrrolidines as catalysts for asymmetric Michael additions of aldehydes to nitroolefins. Chem. Eur. J., 2010, 16(42), 12549-12552.
    • (2010) Chem. Eur. J , vol.16 , Issue.42 , pp. 12549-12552
    • Husmann, R.1    Jörres, M.2    Raabe, G.3    Bolm, C.4
  • 67
    • 70349245000 scopus 로고    scopus 로고
    • Chiral 2-aminobenzimidazoles as recoverable organocatalysts for the addition of 1,3-dicarbonyl compounds to nitroalkenes
    • Almaşi, D.; Alonso, D.A.; Gómez-Bengoa, E.; Nájera, C. Chiral 2-aminobenzimidazoles as recoverable organocatalysts for the addition of 1,3-dicarbonyl compounds to nitroalkenes. J. Org. Chem., 2009, 74, 6163-6168.
    • (2009) J. Org. Chem , vol.74 , pp. 6163-6168
    • Almaşi, D.1    Alonso, D.A.2    Gómez-Bengoa, E.3    Nájera, C.4
  • 68
    • 78349269464 scopus 로고    scopus 로고
    • Sugar-based pyrrolidine as a highly enantioselective organocatalyst for asymmetric Michael addition of ketones to nitrostyrenes
    • Wang, L.; Liu, J.; Miao, T.; Zhou, W.; Li, P.; Ren, K. Zhang, X. Sugar-based pyrrolidine as a highly enantioselective organocatalyst for asymmetric Michael addition of ketones to nitrostyrenes. Adv. Synth. Catal., 2010, 352(14-15), 2571-2578.
    • (2010) Adv. Synth. Catal , vol.352 , Issue.14-15 , pp. 2571-2578
    • Wang, L.1    Liu, J.2    Miao, T.3    Zhou, W.4    Li, P.5    Ren, K.6    Zhang, X.7
  • 69
    • 79957580049 scopus 로고    scopus 로고
    • Chiral squaramide-catalyzed highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes
    • Yang, W.; Du, D.-M. Chiral squaramide-catalyzed highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes. Adv. Synth. Catal., 2011, 353, 1241-1246.
    • (2011) Adv. Synth. Catal , vol.353 , pp. 1241-1246
    • Yang, W.1    Du, D.-M.2
  • 70
    • 78651322223 scopus 로고    scopus 로고
    • 4-Aminothioureaprolinal dithioacetal as a catalyst for highly enantioselective Michael additions of ketones and aldehydes to nitroolefins
    • Chuan, Y.-M.; Yin, L.-Y.; Zhang, Y.-M.; Peng, Y.-G. 4-Aminothioureaprolinal dithioacetal as a catalyst for highly enantioselective Michael additions of ketones and aldehydes to nitroolefins. Eur. J. Org. Chem., 2011, (3), 578-583.
    • (2011) Eur. J. Org. Chem , Issue.3 , pp. 578-583
    • Chuan, Y.-M.1    Yin, L.-Y.2    Zhang, Y.-M.3    Peng, Y.-G.4
  • 71
    • 79953698407 scopus 로고    scopus 로고
    • Thiophosphoramide catalyzed asymmetric Michael addition of cyclopentanone to chalcones
    • Liu, Y.; Wu, Y.; Lu, A.; Wang, Y.; Wu, G.; Zhou, Z.; Tang, C. Thiophosphoramide catalyzed asymmetric Michael addition of cyclopentanone to chalcones. Tetrahedron: Asymmetry, 2011, 22(4), 476-479.
    • (2011) Tetrahedron: Asymmetry , vol.22 , Issue.4 , pp. 476-479
    • Liu, Y.1    Wu, Y.2    Lu, A.3    Wang, Y.4    Wu, G.5    Zhou, Z.6    Tang, C.7
  • 72
    • 61849117439 scopus 로고    scopus 로고
    • α, β-diarylprolinols: Bifunctional organocatalysts for asymmetryc synthesis
    • Lattanzi, A. α, β-diarylprolinols: bifunctional organocatalysts for asymmetryc synthesis. Chem. Commun., 2009, 1452-1463.
    • (2009) Chem. Commun , pp. 1452-1463
    • Lattanzi, A.1
  • 73
    • 84862778055 scopus 로고    scopus 로고
    • Asymmetric triple cascade organocatalytic reaction in water: Construction of polyfunctional cyclohexene building blocks having multiple stereocenters
    • Jia, Y.; Mao, Z.; Wang, R. Asymmetric triple cascade organocatalytic reaction in water: construction of polyfunctional cyclohexene building blocks having multiple stereocenters. Tetrahedron: Asymmetry, 2011, 22, 2018-2023.
    • (2011) Tetrahedron: Asymmetry , vol.22 , pp. 2018-2023
    • Jia, Y.1    Mao, Z.2    Wang, R.3
  • 74
    • 84856626214 scopus 로고    scopus 로고
    • Hexafluorobenzene: A powerful solvent for a noncovalent stereoselective organocatalytic Michael addition reaction
    • Lattanzi, A.; De Fusco, C.; Russo, A.; Poater, A.; Cavallo, L. Hexafluorobenzene: a powerful solvent for a noncovalent stereoselective organocatalytic Michael addition reaction. Chem. Commun., 2012, 48, 1650-1652.
    • (2012) Chem. Commun , vol.48 , pp. 1650-1652
    • Lattanzi, A.1    de Fusco, C.2    Russo, A.3    Poater, A.4    Cavallo, L.5
  • 75
    • 85050272509 scopus 로고
    • Asymmetric catalysis by alkaloids
    • Wynberg, H. Asymmetric catalysis by alkaloids. Top. Stereochem. 1986, 16, 87-129.
    • (1986) Top. Stereochem , vol.16 , pp. 87-129
    • Wynberg, H.1
  • 76
    • 4043154104 scopus 로고    scopus 로고
    • Highly enantioselective conjugate addition of malonate and β-ketoester to nitroalkenes: Asymmetric C-C bond formation with new bifunctional organic catalysts based on cinchona alkaloids
    • Li, H., Wang, Y.; Tang, L.; Deng, L. Highly enantioselective conjugate addition of malonate and β-ketoester to nitroalkenes: asymmetric C-C bond formation with new bifunctional organic catalysts based on cinchona alkaloids. J. Am. Chem. Soc., 2004, 126, 9906-9907.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 9906-9907
    • Li, H.1    Wang, Y.2    Tang, L.3    Deng, L.4
  • 77
    • 62949120090 scopus 로고    scopus 로고
    • Recyclable organocatalysis: Highly enantioselective Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins
    • Tan, B.; Zhang, X.; Chua, P.J.; Zhong, G. Recyclable organocatalysis: highly enantioselective Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins. Chem. Commun., 2009, 779-781.
    • (2009) Chem. Commun , pp. 779-781
    • Tan, B.1    Zhang, X.2    Chua, P.J.3    Zhong, G.4
  • 78
    • 78650570854 scopus 로고    scopus 로고
    • Direct asymmetric vinylogous Michael addition of cyclic enones to nitroalkenes via dienamine catalysis
    • Bencivenni, G.; Galzerano, P.; Mazzanti, A.; Bartoli, G.; Melchiorre, P. Direct asymmetric vinylogous Michael addition of cyclic enones to nitroalkenes via dienamine catalysis. PNAS, 2010, 107(48), 20642-20647.
    • (2010) PNAS , vol.107 , Issue.48 , pp. 20642-20647
    • Bencivenni, G.1    Galzerano, P.2    Mazzanti, A.3    Bartoli, G.4    Melchiorre, P.5
  • 79
    • 77749255393 scopus 로고    scopus 로고
    • Novel thiourea-amine bifunctional catalysts for asymmetric conjugate addition of ketones/aldehydes to nitroalkenes: Rational structural combination for high catalytic efficiency
    • Chen, J.-R.; Cao, Y.-J.; Zou, Y.-Q.; Tan, F.; Fu, L.; Zhu, X.-Y.; Xiao, W.-J. Novel thiourea-amine bifunctional catalysts for asymmetric conjugate addition of ketones/aldehydes to nitroalkenes: rational structural combination for high catalytic efficiency. Org. Biomol. Chem., 2010, 8, 1275-1279.
    • (2010) Org. Biomol. Chem , vol.8 , pp. 1275-1279
    • Chen, J.-R.1    Cao, Y.-J.2    Zou, Y.-Q.3    Tan, F.4    Fu, L.5    Zhu, X.-Y.6    Xiao, W.-J.7
  • 80
    • 58949092249 scopus 로고    scopus 로고
    • Asymmetric Michael addition mediated by novel cinchona alkaloid-derived bifunctional catalysts containing sulfonamides
    • Luo, J.; Xu, L-W.; Hay, R.A.S.; Lu, Y. Asymmetric Michael addition mediated by novel cinchona alkaloid-derived bifunctional catalysts containing sulfonamides. Org. Lett., 2009, 11(2), 437-440.
    • (2009) Org. Lett , vol.11 , Issue.2 , pp. 437-440
    • Luo, J.1    Xu, L.-W.2    Hay, R.A.S.3    Lu, Y.4
  • 81
    • 78650383618 scopus 로고    scopus 로고
    • Catalityc asymmetric domino Michael addition-alkylation reaction: Enantioselective synthesis of dihydrofurans
    • Rueping, M.; Parra, A.; Uria, U.; Besselièvre, F.; Merino, E. Catalityc asymmetric domino Michael addition-alkylation reaction: enantioselective synthesis of dihydrofurans. Org. Lett., 2010, 12(24), 5680-5683.
    • (2010) Org. Lett , vol.12 , Issue.24 , pp. 5680-5683
    • Rueping, M.1    Parra, A.2    Uria, U.3    Besselièvre, F.4    Merino, E.5
  • 82
    • 82155176175 scopus 로고    scopus 로고
    • Facile construction of vicinal quaternary and tertiary stereocenters via region-and stereoselective organocatalytic Michael addition to nitrodienes
    • Chauhan, P.; Chimni, S.S. Facile construction of vicinal quaternary and tertiary stereocenters via region-and stereoselective organocatalytic Michael addition to nitrodienes. Adv. Synth. Catal., 2011, 353, 3203-3212.
    • (2011) Adv. Synth. Catal , vol.353 , pp. 3203-3212
    • Chauhan, P.1    Chimni, S.S.2
  • 83
    • 55549133297 scopus 로고    scopus 로고
    • Chiral squaramide derivatives are excellent hydrogen bond donor catalyst
    • Malerich, J.P.; Hagihara, K.; Rawal, V.H. Chiral squaramide derivatives are excellent hydrogen bond donor catalyst. J. Am Chem. Soc., 2008, 130, 14416-14417.
    • (2008) J. Am Chem. Soc , vol.130 , pp. 14416-14417
    • Malerich, J.P.1    Hagihara, K.2    Rawal, V.H.3
  • 84
    • 80051756054 scopus 로고    scopus 로고
    • Hydrogen bonding mediated enantioselective organocatalysis in brine: Significant rate acceleration and enhanced stereoselectivity in enantioselective Michael addition reactions of 1,3-dicarbonyls to β-nitroolefins
    • Bae, H.-Y.; Some, S.; Oh, J.-S.; Lee, Y.-S., Song, C.-E. Hydrogen bonding mediated enantioselective organocatalysis in brine: significant rate acceleration and enhanced stereoselectivity in enantioselective Michael addition reactions of 1,3-dicarbonyls to β-nitroolefins. Chem. Commun., 2011, 47, 9621-9623.
    • (2011) Chem. Commun , vol.47 , pp. 9621-9623
    • Bae, H.-Y.1    Some, S.2    Oh, J.-S.3    Lee, Y.-S.4    Song, C.-E.5
  • 85
    • 80054731675 scopus 로고    scopus 로고
    • 3-Symmetrical cinchonine-squaramide as new highly efficient, and recyclable organocatalyst for enantioselective Michael addition
    • 3-Symmetrical cinchonine-squaramide as new highly efficient, and recyclable organocatalyst for enantioselective Michael addition. Adv. Synth. Catal., 2011, 353, 2715-2720.
    • (2011) Adv. Synth. Catal , vol.353 , pp. 2715-2720
    • Min, C.1    Han, X.2    Liao, Z.3    Wu, X.4    Zhou, H.-B.5    Dong, C.6
  • 86
    • 11844302258 scopus 로고    scopus 로고
    • Enantio-and diasteroselective Michael reaction of 1,3-dicarbonyl compounds to nitroolefins catalyzed by a bifunctional thiourea
    • Okino, T.; Hoashi, Y.; Furakawa, T.; Xu, X.; Takemoto, Y. Enantio-and diasteroselective Michael reaction of 1,3-dicarbonyl compounds to nitroolefins catalyzed by a bifunctional thiourea. J. Am Chem. Soc., 2005, 127, 119-125.
    • (2005) J. Am Chem. Soc , vol.127 , pp. 119-125
    • Okino, T.1    Hoashi, Y.2    Furakawa, T.3    Xu, X.4    Takemoto, Y.5
  • 87
    • 33746323982 scopus 로고    scopus 로고
    • Thiourea-catalyzed asymmetric Michael addition of activated methylene compounds to α, β-unsaturated imides: Dual activation of imide by intra-and intermolecular hydrogen bonding
    • Inokuma, T.; Hoashi, Y.; Takemoto, Y. Thiourea-catalyzed asymmetric Michael addition of activated methylene compounds to α, β-unsaturated imides: dual activation of imide by intra-and intermolecular hydrogen bonding. J. Am. Chem. Soc., 2006, 128, 9413-9419.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 9413-9419
    • Inokuma, T.1    Hoashi, Y.2    Takemoto, Y.3
  • 88
    • 33744928626 scopus 로고    scopus 로고
    • Highly enantioselective direct conjugate addition of ketones to nitroalkenes promoted by a chiral primary amine-thiourea catalyst
    • Huang, H., Jacobsen, E.N. Highly enantioselective direct conjugate addition of ketones to nitroalkenes promoted by a chiral primary amine-thiourea catalyst. J. Am Chem. Soc., 2006, 28, 7170-7171.
    • (2006) J. Am Chem. Soc , vol.28 , pp. 7170-7171
    • Huang, H.1    Jacobsen, E.N.2
  • 89
    • 33744782039 scopus 로고    scopus 로고
    • Chiral thiourea-based bifunctional organocatalysts in the asymmetric nitro-Michael addition: A joint experimental-theoretical study
    • Yalalov, D.A.; Tsogoeva, S.B.; Schmatz, S. Chiral thiourea-based bifunctional organocatalysts in the asymmetric nitro-Michael addition: a joint experimental-theoretical study. Adv. Synth. Catal., 2006, 348, 826-832.
    • (2006) Adv. Synth. Catal , vol.348 , pp. 826-832
    • Yalalov, D.A.1    Tsogoeva, S.B.2    Schmatz, S.3
  • 90
    • 33947169944 scopus 로고    scopus 로고
    • Highly enantioselective Michael addition of aromatic ketones to nitroolefins promoted by chiral bifunctional primary amine-thiourea catalysts based on saccharides
    • Liu, K.; Cui, H.-F.; Nie, J.; Dong, K.-Y.; Li, X.-J.; Ma, J.-A. Highly enantioselective Michael addition of aromatic ketones to nitroolefins promoted by chiral bifunctional primary amine-thiourea catalysts based on saccharides. Org. Lett., 2007, 9(5), 923-925.
    • (2007) Org. Lett , vol.9 , Issue.5 , pp. 923-925
    • Liu, K.1    Cui, H.-F.2    Nie, J.3    Dong, K.-Y.4    Li, X.-J.5    Ma, J.-A.6
  • 91
    • 69249186407 scopus 로고    scopus 로고
    • Organocatalytic asymmetric Michael addition of β-ketoesters to nitroalkenes
    • Kwon, B.-K.; Kim, D.-Y. Organocatalytic asymmetric Michael addition of β-ketoesters to nitroalkenes. Bull. Korean Chem. Soc. 2009, 30(7), 1441-1442.
    • (2009) Bull. Korean Chem. Soc , vol.30 , Issue.7 , pp. 1441-1442
    • Kwon, B.-K.1    Kim, D.-Y.2
  • 92
    • 77949292644 scopus 로고    scopus 로고
    • Chiral bifunctional thiourea-catalyzed enantioselective Michael addition of ketones to nitrodienes
    • Ma, H.; Liu, K.; Zhang, F.-G.; Zhu, C.-L.; Nie, J.; Ma, J.-A. Chiral bifunctional thiourea-catalyzed enantioselective Michael addition of ketones to nitrodienes. J. Org. Chem., 2010, 75, 1402-1409.
    • (2010) J. Org. Chem , vol.75 , pp. 1402-1409
    • Ma, H.1    Liu, K.2    Zhang, F.-G.3    Zhu, C.-L.4    Nie, J.5    Ma, J.-A.6
  • 93
    • 67649657963 scopus 로고    scopus 로고
    • Asymmetric conjugate addition of carbonyl compounds to nitroalkenes catalized by chiral bifunctional thioureas
    • Zhang, X.-J.; Liu, S.-P.; Lao, J.-H.; Du, G.-J.; Yan, M.; Chan, A.S.C. Asymmetric conjugate addition of carbonyl compounds to nitroalkenes catalized by chiral bifunctional thioureas. Tetrahedron: Asymmetry, 2009, 20, 1451-1458.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1451-1458
    • Zhang, X.-J.1    Liu, S.-P.2    Lao, J.-H.3    Du, G.-J.4    Yan, M.5    Chan, A.S.C.6
  • 94
    • 67649491244 scopus 로고    scopus 로고
    • Simple cyclohexanediamine-derived primary amine thiourea catalized highly enantioselective conjugate addition of nitroalkanes to enones
    • Mei, K.; Jin, M.; Zhang, S.; Li, P.; Liu, W.; Chen, X.; Xue, F.; Duan, W.; Wang, W. Simple cyclohexanediamine-derived primary amine thiourea catalized highly enantioselective conjugate addition of nitroalkanes to enones. Org. Lett. 2009, 11(13), 2864-2867.
    • (2009) Org. Lett , vol.11 , Issue.13 , pp. 2864-2867
    • Mei, K.1    Jin, M.2    Zhang, S.3    Li, P.4    Liu, W.5    Chen, X.6    Xue, F.7    Duan, W.8    Wang, W.9
  • 95
    • 66149096694 scopus 로고    scopus 로고
    • Higly enantioselective Michael addition of acetone to nitroolefins catalyzed by chiral bifunctional primary aminethiourea catalysts with acetic acid
    • Gu, Q.; Guo, X.-T.; Wu, X.-Y. Higly enantioselective Michael addition of acetone to nitroolefins catalyzed by chiral bifunctional primary aminethiourea catalysts with acetic acid. Tetrahedron, 2009, 65, 5265-5270.
    • (2009) Tetrahedron , vol.65 , pp. 5265-5270
    • Gu, Q.1    Guo, X.-T.2    Wu, X.-Y.3
  • 96
    • 77149143504 scopus 로고    scopus 로고
    • Asymmetric Michael addition reaction of 3-substituted oxindoles to nitroolefins catalyzed by a chiral alkyl-substituted thiourea catalyst
    • Li, X.; Zhang, B.; Xi, Z.-G.; Luo, S.; Cheng, J.-P. Asymmetric Michael addition reaction of 3-substituted oxindoles to nitroolefins catalyzed by a chiral alkyl-substituted thiourea catalyst. Adv. Synth. Catal.; 2010, 352, 416-424.
    • (2010) Adv. Synth. Catal , vol.352 , pp. 416-424
    • Li, X.1    Zhang, B.2    Xi, Z.-G.3    Luo, S.4    Cheng, J.-P.5
  • 97
    • 78951476535 scopus 로고    scopus 로고
    • Self-assembled proline-amino thioureas as a efficient organocatalysts for the asymmetric Michael addition of aldehydes to nitroolefins
    • Wang, W.-H.; Abe, T.; Wang, X.-B.; Kodama, K.; Hirose, T.; Zhang, G.-Y. Self-assembled proline-amino thioureas as a efficient organocatalysts for the asymmetric Michael addition of aldehydes to nitroolefins. Tetrahedron: Asymmetry, 2010, 21, 2925-2933.
    • (2010) Tetrahedron: Asymmetry , vol.21 , pp. 2925-2933
    • Wang, W.-H.1    Abe, T.2    Wang, X.-B.3    Kodama, K.4    Hirose, T.5    Zhang, G.-Y.6
  • 98
    • 33746643770 scopus 로고    scopus 로고
    • Pyrrolidine-thiourea as a bifunctional organocatalyst: Highly enantioselective Michael addition of cyclohexanone to nitroolefins
    • Cao, C.-L.; Ye, M.-C.; Sun, X.-L.; Tang, Y. Pyrrolidine-thiourea as a bifunctional organocatalyst: Highly enantioselective Michael addition of cyclohexanone to nitroolefins. Org. Lett., 2006, 8(14), 2901-2904.
    • (2006) Org. Lett , vol.8 , Issue.14 , pp. 2901-2904
    • Cao, C.-L.1    Ye, M.-C.2    Sun, X.-L.3    Tang, Y.4
  • 99
    • 33751407719 scopus 로고    scopus 로고
    • Michael additions in water of ketones to nitroolefins catalyzed by readily tunable and bifunctional pyrrolidine-thiourea organocatalysts
    • Cao, Y.-J.; Lai, Y.-Y.; Wang, X.; Li, Y.-J.; Xiao, W.-J. Michael additions in water of ketones to nitroolefins catalyzed by readily tunable and bifunctional pyrrolidine-thiourea organocatalysts. Tetrahedron Lett., 2007, 48, 21-24.
    • (2007) Tetrahedron Lett , vol.48 , pp. 21-24
    • Cao, Y.-J.1    Lai, Y.-Y.2    Wang, X.3    Li, Y.-J.4    Xiao, W.-J.5
  • 100
    • 34247472031 scopus 로고    scopus 로고
    • Enantioselective and diasteroselective Michael addition of ketone/aldehyde to transnitroolefins catalyzed by a novel chiral pyrrolidine-thiourea
    • Shen, Z.; Zhang, Y.; Jiao, C.; Li, B.; Ding, J.; Zhang, Y. Enantioselective and diasteroselective Michael addition of ketone/aldehyde to transnitroolefins catalyzed by a novel chiral pyrrolidine-thiourea. Chirality, 2007, 19, 307-312.
    • (2007) Chirality , vol.19 , pp. 307-312
    • Shen, Z.1    Zhang, Y.2    Jiao, C.3    Li, B.4    Ding, J.5    Zhang, Y.6
  • 101
    • 77953473284 scopus 로고    scopus 로고
    • Effective asymmetric Michael addition of acetone to nitroalkenes promoted by chiral proline amide-thiourea bifunctional catalyst
    • Wang, Q.-W.; Peng, L.; Fu, J.-Y.; Huang, Q.-C.; Wang, L.-X.; Xu, X.-Y. Effective asymmetric Michael addition of acetone to nitroalkenes promoted by chiral proline amide-thiourea bifunctional catalyst. ARKIVOC, 2010, ii, 340-351.
    • (2010) ARKIVOC , vol.2 , pp. 340-351
    • Wang, Q.-W.1    Peng, L.2    Fu, J.-Y.3    Huang, Q.-C.4    Wang, L.-X.5    Xu, X.-Y.6
  • 102
    • 84858974430 scopus 로고    scopus 로고
    • Efficient enantioselective Michael addition of nitroalkenes catalyzed by a surfactant-type bifunctional thiourea organocatalyst in the presence of water
    • Li, J.; Liu, Y.; Liu, L. Efficient enantioselective Michael addition of nitroalkenes catalyzed by a surfactant-type bifunctional thiourea organocatalyst in the presence of water. Lett. Org. Chem., 2012, 9, 51-55.
    • (2012) Lett. Org. Chem , vol.9 , pp. 51-55
    • Li, J.1    Liu, Y.2    Liu, L.3
  • 103
    • 77954309580 scopus 로고    scopus 로고
    • Highly enantioselective Michael addition of aldehydes to nitroolefins catalyzed by primary amine thiourea organocatalysts
    • Chen, J.-R.; Zou, Y.-Q.; Fu, L.; Ren, F.; Tan, F.; Xiao, W.-J. Highly enantioselective Michael addition of aldehydes to nitroolefins catalyzed by primary amine thiourea organocatalysts. Tetrahedron, 2010, 66, 5367-5372.
    • (2010) Tetrahedron , vol.66 , pp. 5367-5372
    • Chen, J.-R.1    Zou, Y.-Q.2    Fu, L.3    Ren, F.4    Tan, F.5    Xiao, W.-J.6
  • 104
    • 77953447483 scopus 로고    scopus 로고
    • Asymmetric organocatalytic Michael addition of Meldruḿs acid to nitroalkenes: Probing the mechanism of bifunctional thiourea organocatalysts
    • Kataja, A.O.; Koskinen, A.M.P. Asymmetric organocatalytic Michael addition of Meldruḿs acid to nitroalkenes: Probing the mechanism of bifunctional thiourea organocatalysts. ARKIVOC, 2010, ii, 205-223.
    • (2010) ARKIVOC , vol.2 , pp. 205-223
    • Kataja, A.O.1    Koskinen, A.M.P.2
  • 105
    • 14844316261 scopus 로고    scopus 로고
    • Direct, highly enantioselective pyrrolidine sulfonamide catalyzed Michael addition of aldehydes to nitrostyrenes
    • Wang, W.; Wang, J.; Li, H. Direct, highly enantioselective pyrrolidine sulfonamide catalyzed Michael addition of aldehydes to nitrostyrenes. Angew. Chem. Int. Ed., 2005, 44, 1369-1371.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 1369-1371
    • Wang, W.1    Wang, J.2    Li, H.3
  • 106
    • 77956338488 scopus 로고    scopus 로고
    • Functionalized proline with double hydrogen bonding potential: Highly enantioselectve Michael addition of carbonyl compounds to β-nitrostyrenes in brine
    • Saha, S.; Seth, S.; Moorthy, J.N. Functionalized proline with double hydrogen bonding potential: highly enantioselectve Michael addition of carbonyl compounds to β-nitrostyrenes in brine. Tetrahedron Lett., 2010, 51, 5281-5286.
    • (2010) Tetrahedron Lett , vol.51 , pp. 5281-5286
    • Saha, S.1    Seth, S.2    Moorthy, J.N.3
  • 107
    • 34447558355 scopus 로고    scopus 로고
    • Highly enantioselective Michael addition of ketones to nitroolefins catalyzed by (S)-pyrrolidine arenesulfonamide
    • Ni, B.; Zhang, Q.; Headley, A.D. Highly enantioselective Michael addition of ketones to nitroolefins catalyzed by (S)-pyrrolidine arenesulfonamide Tetrahedron:Asymmetry, 2007, 18, 1443-1447.
    • (2007) Tetrahedron:Asymmetry , vol.18 , pp. 1443-1447
    • Ni, B.1    Zhang, Q.2    Headley, A.D.3
  • 108
    • 79959790565 scopus 로고    scopus 로고
    • Pyrrolidinyl-sulfonamide derivatives as a new class of bifunctional organocatalysts for direct asymmetric Michael addition of cyclohexanone to nitroalkenes
    • Chen, J.-R.; Fu, L.; Zou, Y.-Q.; Chang, N.-J.; Rong, J.; Xiao, W.-J. Pyrrolidinyl-sulfonamide derivatives as a new class of bifunctional organocatalysts for direct asymmetric Michael addition of cyclohexanone to nitroalkenes. Org. Biomol. Chem., 2011, 9, 5280-5287.
    • (2011) Org. Biomol. Chem , vol.9 , pp. 5280-5287
    • Chen, J.-R.1    Fu, L.2    Zou, Y.-Q.3    Chang, N.-J.4    Rong, J.5    Xiao, W.-J.6
  • 109
  • 110
    • 77949819508 scopus 로고    scopus 로고
    • Noyorís Ts-DPEN ligand: Simple yet effective catalyst for the highly enantioselective Michael addition of acetone to nitroalkenes
    • Peng, L.; Xu, X.-Y.; Wang, L.-L.; Huang, J.; Bai, J.-F.; Huang, Q.-C., Wang, L.-X. Noyorís Ts-DPEN ligand: Simple yet effective catalyst for the highly enantioselective Michael addition of acetone to nitroalkenes. Eur. J. Org. Chem., 2010, (10), 1849-1853.
    • (2010) Eur. J. Org. Chem , Issue.10 , pp. 1849-1853
    • Peng, L.1    Xu, X.-Y.2    Wang, L.-L.3    Huang, J.4    Bai, J.-F.5    Huang, Q.-C.6    Wang, L.-X.7
  • 111
    • 33750294019 scopus 로고    scopus 로고
    • 2-symetric bis(sulfonamide)-cyclohexane-1,2-diamine-RhCp* complex and its application in the asymmetric transfer hydrogenation (ATH) of ketones in water
    • 2-symetric bis(sulfonamide)-cyclohexane-1,2-diamine-RhCp* complex and its application in the asymmetric transfer hydrogenation (ATH) of ketones in water. Tetrahedron Lett., 2006, 47, 8515-8518.
    • (2006) Tetrahedron Lett , vol.47 , pp. 8515-8518
    • Cortez, N.A.1    Rodríguez-Apodaca, R.2    Aguirre, G.3    Parra-Hake, M.4    Cole, T.5    Somanathan, R.6
  • 112
    • 34248647281 scopus 로고    scopus 로고
    • Water-soluble chiral monosulfonamide-cyclohexane-1,2-diamine-RhCp* complex and its application in the asymmetric transfer hydrogenation (ATH) of ketones
    • Cortez, N.A.; Aguirre, G.; Parra-Hake, M.; Somanathan, R. Water-soluble chiral monosulfonamide-cyclohexane-1,2-diamine-RhCp* complex and its application in the asymmetric transfer hydrogenation (ATH) of ketones. Tetrahedron Lett., 2007, 48, 4335-4338.
    • (2007) Tetrahedron Lett , vol.48 , pp. 4335-4338
    • Cortez, N.A.1    Aguirre, G.2    Parra-Hake, M.3    Somanathan, R.4
  • 113
    • 47049114954 scopus 로고    scopus 로고
    • Ruthenium(II) and rhodium(III) catalyzed asymmetric transfer hydrogenation (ATH) of acetophenone in isopropanol and in aqueous sodium formate using new chiral substituted aromatic monosulfonamide ligands derived from (1R,2R)-diaminecyclohexane
    • Cortez, N.A.; Aguirre, G.; Parra-Hake, M.; Somanathan, R. Ruthenium(II) and rhodium(III) catalyzed asymmetric transfer hydrogenation (ATH) of acetophenone in isopropanol and in aqueous sodium formate using new chiral substituted aromatic monosulfonamide ligands derived from (1R,2R)-diaminecyclohexane. Tetrahedron: Asymmetry, 2008, 19, 1304-1309.
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 1304-1309
    • Cortez, N.A.1    Aguirre, G.2    Parra-Hake, M.3    Somanathan, R.4
  • 114
    • 78650319007 scopus 로고    scopus 로고
    • Practical synthesis of optically active alcohols via asymmetric transfer hydrogenation of aromatic ketones using chiral Rh(III)-monosulfonamide ligand complex in aqueous media
    • Cortez, N.A.; Aguirre, G.; Parra-Hake, M.; Somanathan, R.; Arita, A.J.; Cooksy, A.L.; Anaya de Parrodi, C.; Huelgas, G. Practical synthesis of optically active alcohols via asymmetric transfer hydrogenation of aromatic ketones using chiral Rh(III)-monosulfonamide ligand complex in aqueous media. Synth. Commun., 2011, 41, 73-84.
    • (2011) Synth. Commun , vol.41 , pp. 73-84
    • Cortez, N.A.1    Aguirre, G.2    Parra-Hake, M.3    Somanathan, R.4    Arita, A.J.5    Cooksy, A.L.6    Anaya de Parrodi, C.7    Huelgas, G.8
  • 115
    • 84862800781 scopus 로고    scopus 로고
    • Enantioselective conjugate addition of ketones to nitroalkenes catalyzed by pyrrolidine-sulfamides
    • Wang J.; Lao, J.; Du, Q.; Nie, S.; Hu, Z.; Yan, M. Enantioselective conjugate addition of ketones to nitroalkenes catalyzed by pyrrolidine-sulfamides. CHRALITY 2012, 24, 232-238.
    • (2012) CHRALITY , vol.24 , pp. 232-238
    • Wang, J.1    Lao, J.2    Du, Q.3    Nie, S.4    Hu, Z.5    Yan, M.6
  • 119
    • 47749137879 scopus 로고    scopus 로고
    • Supported proline and prolinederivatives as recyclable organocatalysts
    • Gruttadauria, M.; Giacalone, F.; Noto, R. Supported proline and prolinederivatives 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
  • 120
    • 77952986153 scopus 로고    scopus 로고
    • Polymer-supported chiral organocatalysts: Synthetic strategies for the road towards affordable polymeric immobilization
    • Kristensen, T. E.; Hansen, T. Polymer-supported chiral organocatalysts: synthetic strategies for the road towards affordable polymeric immobilization. Eur. J. Org. Chem., 2010, (17), 3179-3204
    • (2010) Eur. J. Org. Chem , Issue.17 , pp. 3179-3204
    • Kristensen, T.E.1    Hansen, T.2
  • 121
    • 79957554606 scopus 로고    scopus 로고
    • Efficient recovery and reuse of an immobilized peptidic organocatalyst
    • Arakawa, Y.; Wiesner, M.; Wennemers, H. Efficient recovery and reuse of an immobilized peptidic organocatalyst. Adv. Synth. Catal., 2011, 353(8), 1201-1206.
    • (2011) Adv. Synth. Catal , vol.353 , Issue.8 , pp. 1201-1206
    • Arakawa, Y.1    Wiesner, M.2    Wennemers, H.3
  • 122
    • 73349125422 scopus 로고    scopus 로고
    • A highly selective, polymer-supported organocatalyst for Michael additions with enzyme-like behavior
    • Alza, E.; Pericás, M. A. A highly selective, polymer-supported organocatalyst for Michael additions with enzyme-like behavior. Adv. Synth. Catal., 2009, 351(18), 3051-3056.
    • (2009) Adv. Synth. Catal , vol.351 , Issue.18 , pp. 3051-3056
    • Alza, E.1    Pericás, M.A.2
  • 123
    • 65449174801 scopus 로고    scopus 로고
    • Highly enantioselective Michael addition reactions in water catalyzed by an insoluble MPS-supported 4-sulfonamidyl prolinol tert-butyldiphenylsilyl ether
    • Chuan, Y.; Chen, G.; Peng, Y. Highly enantioselective Michael addition reactions in water catalyzed by an insoluble MPS-supported 4-sulfonamidyl prolinol tert-butyldiphenylsilyl ether. Tetrahedron Lett., 2009, 50(25), 3054-3058.
    • (2009) Tetrahedron Lett , vol.50 , Issue.25 , pp. 3054-3058
    • Chuan, Y.1    Chen, G.2    Peng, Y.3
  • 124
    • 50849092526 scopus 로고    scopus 로고
    • Asymmetric epoxidation, Michael addition, and triple cascade reaction using polymer-supported prolinol-based auxiliaries
    • Varela, M.C.; Dixon, S.M.; Lam, K.S.; Schore, N.E. Asymmetric epoxidation, Michael addition, and triple cascade reaction using polymer-supported prolinol-based auxiliaries. Tetrahedron, 2008, 64(43), 10087-10090.
    • (2008) Tetrahedron , vol.64 , Issue.43 , pp. 10087-10090
    • Varela, M.C.1    Dixon, S.M.2    Lam, K.S.3    Schore, N.E.4
  • 125
    • 81855192747 scopus 로고    scopus 로고
    • Prolinamide bridged silsesquioxane as an efficient, ecocompatible and recyclable chiral organocatalyst
    • Monge-Marcet, A.; Pleixats, R.; Cattoën, X.; Man, M. W. C.; Alonso, D. A.; Nájera, C. Prolinamide bridged silsesquioxane as an efficient, ecocompatible and recyclable chiral organocatalyst. New J. Chem., 2011, 35, 2766-2772.
    • (2011) New J. Chem , vol.35 , pp. 2766-2772
    • Monge-Marcet, A.1    Pleixats, R.2    Cattoën, X.3    Man, M.W.C.4    Alonso, D.A.5    Nájera, C.6
  • 126
    • 58649116475 scopus 로고    scopus 로고
    • Are ionic liquids suitable media for organocatalytic reactions?
    • Toma, Š.; Mečiarová, M.; Šebesta, R. Are ionic liquids suitable media for organocatalytic reactions? Eur. J. Org. Chem., 2009, (3), 321-327.
    • (2009) Eur. J. Org. Chem , Issue.3 , pp. 321-327
    • Toma, S.1    Mečiarová, M.2    Šebesta, R.3
  • 127
    • 68349143232 scopus 로고    scopus 로고
    • Functionalized chiral ionic liquids: A new type of asymmetric organocatalysts and nonclassical chiral ligands
    • Luo, S.; Zhang, L.; Cheng, J.-P. Functionalized chiral ionic liquids: A new type of asymmetric organocatalysts and nonclassical chiral ligands. Chem. Asian J., 2009, 4(8), 1184-1195.
    • (2009) Chem. Asian J , vol.4 , Issue.8 , pp. 1184-1195
    • Luo, S.1    Zhang, L.2    Cheng, J.-P.3
  • 128
    • 78649330635 scopus 로고    scopus 로고
    • 4]: As a recyclable and highly efficient organocatalyst for asymmetric Michael addition reactions
    • 4]: as a recyclable and highly efficient organocatalyst for asymmetric Michael addition reactions. Tetrahedron: Asymmetry, 2010, 21(20), 2530-2534.
    • (2010) Tetrahedron: Asymmetry , vol.21 , Issue.20 , pp. 2530-2534
    • Xu, D.-Z.1    Liu, Y.2    Shi, S.3    Wang, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.