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Volumn 15, Issue 24, 2011, Pages 4046-4082

Enantioselective organocatalytic synthesis of 5 and 6 membered heterocycles

Author keywords

Diels alder; Domino reaction; Michael reaction; Organocatalysis

Indexed keywords

ADDITION REACTIONS; CATALYSIS; ENANTIOSELECTIVITY;

EID: 81255211559     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211798109213     Document Type: Article
Times cited : (11)

References (109)
  • 1
    • 0034654216 scopus 로고    scopus 로고
    • Proline-catalyzed direct asymmetric aldol reactions
    • List, B.; Lerner, R. A.; Barbas, C. F., III. Proline-Catalyzed Direct Asymmetric Aldol Reactions. J. Am. Chem. Soc. 2000, 122, 2395-2396.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 2395-2396
    • List, B.1    Lerner, R.A.2    Barbas III, C.F.3
  • 2
    • 0034600250 scopus 로고    scopus 로고
    • New strategies for organic catalysis: The first highly enantioselective organocatalytic diels-alder reaction
    • Ahrendt, K. A.; Borths, C. J.; MacMillan, D. W. C. New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels-Alder Reaction. J. Am. Chem. Soc. 2000, 122, 4243-4244.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 4243-4244
    • Ahrendt, K.A.1    Borths, C.J.2    Macmillan, D.W.C.3
  • 3
    • 85017168755 scopus 로고    scopus 로고
    • Most relevant recent enantioselective synthesis of pyrrolidines and piperidines
    • Companyo, X.; Alba, A.-N.; Rios, R., Most relevant recent enantioselective synthesis of pyrrolidines and piperidines. Targets in Heterocyclic Systems 2009, 13, 147-174.
    • (2009) Targets in Heterocyclic Systems , vol.13 , pp. 147-174
    • Companyo, X.1    Alba, A.-N.2    Rios, R.3
  • 4
    • 1842732181 scopus 로고    scopus 로고
    • Enantioselective organocatalytic construction of pyrroloindolines by a cascade addition-cyclization strategy: Synthesis of (-)-flustramine B
    • Austin, J. F.; Kim, S.-G.; Sinz, C. J.; Xiao, W.-J.; MacMillan, D. W. C., Enantioselective organocatalytic construction of pyrroloindolines by a cascade addition-cyclization strategy: synthesis of (-)-flustramine B. Proc. Natl. Acad. Sci. U. S. A. 2004, 101 (15), 5482-5487
    • (2004) Proc. Natl. Acad. Sci. U. S. A. , vol.101 , Issue.15 , pp. 5482-5487
    • Austin, J.F.1    Kim, S.-G.2    Sinz, C.J.3    Xiao, W.-J.4    Macmillan, D.W.C.5
  • 5
    • 34447315556 scopus 로고    scopus 로고
    • Organocatalytic enantioselective 3+2 cycloaddition of azomethine ylides and alpha,betaunsaturated aldehydes
    • Vicario, J. L.; Reboredo, S.; Badia, D.; Carrillo, L., Organocatalytic enantioselective 3+2 cycloaddition of azomethine ylides and alpha,betaunsaturated aldehydes. Angewandte Chemie-International Edition 2007, 46, 5168-5170.
    • (2007) Angewandte Chemie-International Edition , vol.46 , pp. 5168-5170
    • Vicario, J.L.1    Reboredo, S.2    Badia, D.3    Carrillo, L.4
  • 6
    • 34547682312 scopus 로고    scopus 로고
    • Organocatalytic asymmetric multi-component C+NC+CC synthesis of highly functionalized pyrrolidine derivatives
    • Ibrahem, I.; Rios, R.; Vesely, J.; Córdova, A., Organocatalytic asymmetric multi-component C+NC+CC synthesis of highly functionalized pyrrolidine derivatives. Tetrahedron Lett. 2007, 48 (36), 6252-6257.
    • (2007) Tetrahedron Lett , vol.48 , Issue.36 , pp. 6252-6257
    • Ibrahem, I.1    Rios, R.2    Vesely, J.3    Córdova, A.4
  • 7
    • 35748967901 scopus 로고    scopus 로고
    • Organocatalytic asymmetric 5-hydroxypyrrolidine synthesis: A highly enantioselective route to 3-substituted proline derivatives
    • Rios, R.; Ibrahem, I.; Vesely, J.; Sunden, H.; Córdova, A., Organocatalytic asymmetric 5-hydroxypyrrolidine synthesis: a highly enantioselective route to 3-substituted proline derivatives. Tetrahedron Lett. 2007, 48 (49), 8695-8699.
    • (2007) Tetrahedron Lett , vol.48 , Issue.49 , pp. 8695-8699
    • Rios, R.1    Ibrahem, I.2    Vesely, J.3    Sunden, H.4    Córdova, A.5
  • 8
    • 33846126231 scopus 로고    scopus 로고
    • Organocatalytic asymmetric michael addition of aldehydes to beta -nitroacrolein dimethyl acetal
    • Reyes, E.; Vicario, J. L.; Badia, D.; Carrillo, L., Organocatalytic Asymmetric Michael Addition of Aldehydes to beta -Nitroacrolein Dimethyl Acetal. Org. Lett. 2006, 8 (26), 6135-6138
    • (2006) Org. Lett. , vol.8 , Issue.26 , pp. 6135-6138
    • Reyes, E.1    Vicario, J.L.2    Badia, D.3    Carrillo, L.4
  • 9
    • 55149106147 scopus 로고    scopus 로고
    • Organocatalytic enantioselective synthesis of highly functionalized polysubstituted pyrrolidines
    • Ruiz, N.; Reyes, E.; Vicario, J. L.; Badia, D.; Carrillo, L.; Uria, U., Organocatalytic Enantioselective Synthesis of Highly Functionalized Polysubstituted Pyrrolidines. Chemistry-a European Journal 2008, 14 (30), 9357-9367
    • (2008) Chemistry-a European Journal , vol.14 , Issue.30 , pp. 9357-9367
    • Ruiz, N.1    Reyes, E.2    Vicario, J.L.3    Badia, D.4    Carrillo, L.5    Uria, U.6
  • 10
    • 46849122706 scopus 로고    scopus 로고
    • Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: Enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid
    • Carlson, E. C.; Rathbone, L. K.; Yang, H.; Collett, N. D.; Carter, R. G., Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: Enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid. J. Org. Chem. 2008, 73 (13), 5155-5158
    • (2008) J. Org. Chem. , vol.73 , Issue.13 , pp. 5155-5158
    • Carlson, E.C.1    Rathbone, L.K.2    Yang, H.3    Collett, N.D.4    Carter, R.G.5
  • 11
    • 55849104887 scopus 로고    scopus 로고
    • Highly enantio- and diastereoselective organocatalytic cascade aza-Michael-Michael reactions: A direct method for the synthesis of trisubstituted chiral pyrrolidines
    • Li, H.; Zu, L.; Xie, H.; Wang, J.; Wang, W., Highly enantio- and diastereoselective organocatalytic cascade aza-Michael-Michael reactions: a direct method for the synthesis of trisubstituted chiral pyrrolidines. Chem. Commun. (Cambridge, U. K.) 2008, (43), 5636-5638
    • (2008) Chem. Commun. (Cambridge, U. K.) , Issue.43 , pp. 5636-5638
    • Li, H.1    Zu, L.2    Xie, H.3    Wang, J.4    Wang, W.5
  • 12
    • 41349123337 scopus 로고    scopus 로고
    • The first organocatalytic enantioand diastereoselective 1,3-dipolar cycloaddition of azomethine ylides with nitroalkenes
    • Xue, M. X.; Zhang, X. M.; Gong, L. Z., The first organocatalytic enantioand diastereoselective 1,3-dipolar cycloaddition of azomethine ylides with nitroalkenes. Synlett 2008, (5), 691-694.
    • (2008) Synlett , Issue.5 , pp. 691-694
    • Xue, M.X.1    Zhang, X.M.2    Gong, L.Z.3
  • 13
    • 42649137921 scopus 로고    scopus 로고
    • Asymmetric organocatalytic three-component 1,3-dipolar cycloaddition: Control of stereochemistry via a chiral bronsted acid activated dipole
    • Chen, X.-H.; Zhang, W.-Q.; Gong, L.-Z., Asymmetric Organocatalytic Three-Component 1,3-Dipolar Cycloaddition: Control of Stereochemistry via a Chiral Bronsted Acid Activated Dipole. J. Am. Chem. Soc. 2008, 130 (17), 5652-5653.
    • (2008) J. Am. Chem. Soc. , vol.130 , Issue.17 , pp. 5652-5653
    • Chen, X.-H.1    Zhang, W.-Q.2    Gong, L.-Z.3
  • 14
    • 55449131123 scopus 로고    scopus 로고
    • Reaction control in the organocatalytic asymmetric one-pot, three-component reaction of aldehydes, diethyl alpha-aminomalonate and nitroalkenes: Toward diversity-oriented synthesis
    • Liu, Y. K.; Liu, H.; Du, W.; Yue, L.; Chen, Y. C., Reaction Control in the Organocatalytic Asymmetric One-Pot, Three-Component Reaction of Aldehydes, Diethyl alpha-Aminomalonate and Nitroalkenes: Toward Diversity-Oriented Synthesis. Chemistry-a European Journal 2008, 14 (32), 9873-9877.
    • (2008) Chemistry-a European Journal , vol.14 , Issue.32 , pp. 9873-9877
    • Liu, Y.K.1    Liu, H.2    Du, W.3    Yue, L.4    Chen, Y.C.5
  • 15
    • 56949108837 scopus 로고    scopus 로고
    • Thiourea-catalyzed asymmetric formal [3+2] cycloaddition of azomethine ylides with nitroolefins
    • Xie, J.; Yoshida, K.; Takasu, K.; Takemoto, Y., Thiourea-catalyzed asymmetric formal [3+2] cycloaddition of azomethine ylides with nitroolefins. Tetrahedron Lett. 2008, 49 (48), 6910-6913.
    • (2008) Tetrahedron Lett , vol.49 , Issue.48 , pp. 6910-6913
    • Xie, J.1    Yoshida, K.2    Takasu, K.3    Takemoto, Y.4
  • 16
    • 70349753180 scopus 로고    scopus 로고
    • Nine-step enantioselective total synthesis of (+)-minfiensine
    • Jones, S. B.; Simmons, B.; MacMillan, D. W. C., Nine-Step Enantioselective Total Synthesis of (+)-Minfiensine. J. Am. Chem. Soc. 2009, 131 (38), 13606-13607.
    • (2009) J. Am. Chem. Soc. , vol.131 , Issue.38 , pp. 13606-13607
    • Jones, S.B.1    Simmons, B.2    Macmillan, D.W.C.3
  • 17
    • 66149124126 scopus 로고    scopus 로고
    • Organocatalytic approach to enantioselective one-pot synthesis of pyrrolidine, hexahydropyrrolizine, and octahydroindolizine core structures
    • Wang, Y.-G.; Kumano, T.; Kano, T.; Maruoka, K., Organocatalytic Approach to Enantioselective One-Pot Synthesis of Pyrrolidine, Hexahydropyrrolizine, and Octahydroindolizine Core Structures. Org. Lett. 2009, 11 (9), 2027-2029.
    • (2009) Org. Lett. , vol.11 , Issue.9 , pp. 2027-2029
    • Wang, Y.-G.1    Kumano, T.2    Kano, T.3    Maruoka, K.4
  • 18
    • 70349742473 scopus 로고    scopus 로고
    • Organocatalytic synthesis of spiro [pyrrolidin-3,3'-oxindoles] with high enantiopurity and structural diversity
    • Chen, X.-H.; Wei, Q.; Luo, S.-W.; Xiao, H.; Gong, L.-Z., Organocatalytic Synthesis of Spiro [pyrrolidin-3,3'-oxindoles] with High Enantiopurity and Structural Diversity. J. Am. Chem. Soc. 2009, 131 (38), 13819-13825.
    • (2009) J. Am. Chem. Soc. , vol.131 , Issue.38 , pp. 13819-13825
    • Chen, X.-H.1    Wei, Q.2    Luo, S.-W.3    Xiao, H.4    Gong, L.-Z.5
  • 19
    • 77951106587 scopus 로고    scopus 로고
    • Organocatalytic asymmetric intramolecular [3+2] cycloaddition: A straightforward approach to access multiply substituted hexahydrochromeno [4,3-b]pyrrolidine derivatives in high optical purity
    • Li, N.; Song, J.; Tu, X.-F.; Liu, B.; Chen, X.-H.; Gong, L.-Z., Organocatalytic asymmetric intramolecular [3+2] cycloaddition: A straightforward approach to access multiply substituted hexahydrochromeno [4,3-b]pyrrolidine derivatives in high optical purity. Org. Biomol. Chem. 2010, 8 (9), 2016-2019.
    • (2010) Org. Biomol. Chem. , vol.8 , Issue.9 , pp. 2016-2019
    • Li, N.1    Song, J.2    Tu, X.-F.3    Liu, B.4    Chen, X.-H.5    Gong, L.-Z.6
  • 20
    • 70350676939 scopus 로고    scopus 로고
    • Highly enantioselective catalytic 1,3-dipolar cycloaddition involving 2,3- allenoate dipolarophiles
    • Yu, J.; He, L.; Chen, X.-H.; Song, J.; Chen, W.-J.; Gong, L.-Z., Highly Enantioselective Catalytic 1,3-Dipolar Cycloaddition Involving 2,3- Allenoate Dipolarophiles. Org. Lett. 2009, 11 (21), 4946-4949.
    • (2009) Org. Lett. , vol.11 , Issue.21 , pp. 4946-4949
    • Yu, J.1    He, L.2    Chen, X.-H.3    Song, J.4    Chen, W.-J.5    Gong, L.-Z.6
  • 21
    • 77956581197 scopus 로고    scopus 로고
    • Kinetic resolution of racemic 2,3- allenoates by organocatalytic asymmetric 1,3-dipolar cycloaddition
    • Yu, J.; Chen, W.-J.; Gong, L.-Z., Kinetic Resolution of Racemic 2,3- Allenoates by Organocatalytic Asymmetric 1,3-Dipolar Cycloaddition. Org. Lett. 2010, 12 (18), 4050-4053.
    • (2010) Org. Lett. , vol.12 , Issue.18 , pp. 4050-4053
    • Yu, J.1    Chen, W.-J.2    Gong, L.-Z.3
  • 22
    • 77951095904 scopus 로고    scopus 로고
    • Efficient kinetic resolution of racemic 3-nitro-2H-chromene derivatives catalyzed by Takemoto's organocatalyst
    • Xie, J.-W.; Fan, L.-P.; Su, H.; Li, X.-S.; Xu, D.-C., Efficient kinetic resolution of racemic 3-nitro-2H-chromene derivatives catalyzed by Takemoto's organocatalyst. Org. Biomol. Chem. 2010, 8 (9), 2117-2122.
    • (2010) Org. Biomol. Chem. , vol.8 , Issue.9 , pp. 2117-2122
    • Xie, J.-W.1    Fan, L.-P.2    Su, H.3    Li, X.-S.4    Xu, D.-C.5
  • 23
    • 33749348910 scopus 로고    scopus 로고
    • Organocatalytic and stereoselective [3 + 2] cycloadditions of azomethine imines with alpha, beta -unsaturated aldehydes
    • Chen, W.; Yuan, X.-H.; Li, R.; Du, W.; Wu, Y.; Ding, L.-S.; Chen, Y.-C., Organocatalytic and stereoselective [3 + 2] cycloadditions of azomethine imines with alpha, beta -unsaturated aldehydes. Adv. Synth. Catal. 2006, 348 (14), 1818-1822.
    • (2006) Adv. Synth. Catal. , vol.348 , Issue.14 , pp. 1818-1822
    • Chen, W.1    Yuan, X.-H.2    Li, R.3    Du, W.4    Wu, Y.5    Ding, L.-S.6    Chen, Y.-C.7
  • 24
    • 35048856888 scopus 로고    scopus 로고
    • Enantioselective 1,3-dipolar cycloaddition of cyclic enones catalyzed by multifunctional primary amines: Beneficial effects of hydrogen bonding
    • Chen, W.; Du, W.; Duan, Y.-Z.; Wu, Y.; Yang, S.-Y.; Chen, Y.-C., Enantioselective 1,3-dipolar cycloaddition of cyclic enones catalyzed by multifunctional primary amines: beneficial effects of hydrogen bonding. Angew. Chem., Int. Ed. 2007, 46 (40), 7667-7670.
    • (2007) Angew. Chem., Int. Ed. , vol.46 , Issue.40 , pp. 7667-7670
    • Chen, W.1    Du, W.2    Duan, Y.-Z.3    Wu, Y.4    Yang, S.-Y.5    Chen, Y.-C.6
  • 25
    • 43849090515 scopus 로고    scopus 로고
    • Organocatalytic asymmetric formal [3+2] cycloaddition reaction of isocyanoesters to nitroolefins leading to highly optically active dihydropyrroles
    • Guo, C.; Xue, M.-X.; Zhu, M.-K.; Gong, L.-Z., Organocatalytic asymmetric formal [3+2] cycloaddition reaction of isocyanoesters to nitroolefins leading to highly optically active dihydropyrroles. Angew. Chem., Int. Ed. 2008, 47 (18), 3414-3417.
    • (2008) Angew. Chem., Int. Ed. , vol.47 , Issue.18 , pp. 3414-3417
    • Guo, C.1    Xue, M.-X.2    Zhu, M.-K.3    Gong, L.-Z.4
  • 26
    • 77957164101 scopus 로고    scopus 로고
    • Organocatalytic asymmetric synthesis of chiral pyrrolizines by cascade conjugate addition-aldol reactions
    • Bae, J.-Y.; Lee, H.-J.; Youn, S.-H.; Kwon, S.-H.; Cho, C.-W., Organocatalytic Asymmetric Synthesis of Chiral Pyrrolizines by Cascade Conjugate Addition-Aldol Reactions. Org. Lett. 2010, 12 (19), 4352-4355.
    • (2010) Org. Lett. , vol.12 , Issue.19 , pp. 4352-4355
    • Bae, J.-Y.1    Lee, H.-J.2    Youn, S.-H.3    Kwon, S.-H.4    Cho, C.-W.5
  • 27
    • 77949854636 scopus 로고    scopus 로고
    • Enantioselective synthesis of 3H-Pyrrolo 1,2-a indole-2-carbaldehydes via an Organocatalytic Domino Aza-Michael/Aldol Condensation Reaction
    • Enders, D.; Wang, C.; Raabe, G., Enantioselective Synthesis of 3H-Pyrrolo 1,2-a indole-2-carbaldehydes via an Organocatalytic Domino Aza- Michael/Aldol Condensation Reaction. Synthesis-Stuttgart 2009, (24), 4119-4124.
    • (2009) Synthesis-Stuttgart , Issue.24 , pp. 4119-4124
    • Enders, D.1    Wang, C.2    Raabe, G.3
  • 28
    • 75749154390 scopus 로고    scopus 로고
    • Asymmetric organocatalytic n-alkylation of indole-2-carbaldehydes with alpha,beta-unsaturated aldehydes: One-Pot synthesis of chiral pyrrolo 1,2-a indole-2- carbaldehydes
    • Hong, L.; Sun, W. S.; Liu, C. X.; Wang, L.; Wang, R., Asymmetric Organocatalytic N-Alkylation of Indole-2-carbaldehydes with alpha,beta-Unsaturated Aldehydes: One-Pot Synthesis of Chiral Pyrrolo 1,2-a indole-2- carbaldehydes. Chemistry-a European Journal 2010, 16 (2), 440-444.
    • (2010) Chemistry-a European Journal , vol.16 , Issue.2 , pp. 440-444
    • Hong, L.1    Sun, W.S.2    Liu, C.X.3    Wang, L.4    Wang, R.5
  • 29
    • 70449095147 scopus 로고    scopus 로고
    • Enantioselective one-pot organocatalytic michael addition/gold-catalyzed tandem acetalization/cyclization
    • Belot, S.; Vogt, K. A.; Besnard, C.; Krause, N.; Alexakis, A., Enantioselective One-Pot Organocatalytic Michael Addition/Gold-Catalyzed Tandem Acetalization/Cyclization. Angewandte Chemie-International Edition 2009, 48 (47), 8923-8926.
    • (2009) Angewandte Chemie-International Edition , vol.48 , Issue.47 , pp. 8923-8926
    • Belot, S.1    Vogt, K.A.2    Besnard, C.3    Krause, N.4    Alexakis, A.5
  • 30
    • 77949855662 scopus 로고    scopus 로고
    • Organocatalyzed Conjugate Addition of Carbonyl Compounds to Nitrodienes/Nitroenynes and Synthetic Applications
    • Belot, S.; Quintard, A.; Krause, N.; Alexakis, A., Organocatalyzed Conjugate Addition of Carbonyl Compounds to Nitrodienes/Nitroenynes and Synthetic Applications. Adv. Synth. Catal. 2010, 352 (4), 667-695.
    • (2010) Adv. Synth. Catal. , vol.352 , Issue.4 , pp. 667-695
    • Belot, S.1    Quintard, A.2    Krause, N.3    Alexakis, A.4
  • 31
    • 27144545042 scopus 로고    scopus 로고
    • Efficiency in isotetronic acid synthesis via a diamine-acid couple catalyzed ethyl pyruvate homoaldol reaction
    • Dambruoso, P.; Massi, A.; Dondoni, A., Efficiency in isotetronic acid synthesis via a diamine-acid couple catalyzed ethyl pyruvate homoaldol reaction. Org. Lett. 2005, 7 (21), 4657-4660.
    • (2005) Org. Lett. , vol.7 , Issue.21 , pp. 4657-4660
    • Dambruoso, P.1    Massi, A.2    Dondoni, A.3
  • 33
    • 0034638388 scopus 로고    scopus 로고
    • New strategies for organic catalysis: The first enantioselective organocatalytic 1,3-dipolar cycloaddition
    • Jen, W. S.; Wiener, J. J. M.; MacMillan, D. W. C., New Strategies for Organic Catalysis: The First Enantioselective Organocatalytic 1,3-Dipolar Cycloaddition. J. Am. Chem. Soc. 2000, 122 (40), 9874-9875.
    • (2000) J. Am. Chem. Soc. , vol.122 , Issue.40 , pp. 9874-9875
    • Jen, W.S.1    Wiener, J.J.M.2    Macmillan, D.W.C.3
  • 34
    • 0043157645 scopus 로고    scopus 로고
    • Organocatalysts promote enantioselective 1,3- dipolar cycloadditions of nitrones with 1-cycloalkene-1-carboxaldehydes
    • Karlsson, S.; Hoegberg, H.-E., Organocatalysts promote enantioselective 1,3- dipolar cycloadditions of nitrones with 1-cycloalkene-1-carboxaldehydes. Eur. J. Org. Chem. 2003, (15), 2782-2791.
    • (2003) Eur. J. Org. Chem. , Issue.15 , pp. 2782-2791
    • Karlsson, S.1    Hoegberg, H.-E.2
  • 35
    • 34447268984 scopus 로고    scopus 로고
    • A simple one-pot, three-component, catalytic, highly enantioselective isoxazolidine synthesis
    • Rios, R.; Ibrahem, I.; Vesely, J.; Zhao, G. L.; Córdova, A., A simple one-pot, three-component, catalytic, highly enantioselective isoxazolidine synthesis. Tetrahedron Lett. 2007, 48 (32), 5701-5705.
    • (2007) Tetrahedron Lett , vol.48 , Issue.32 , pp. 5701-5705
    • Rios, R.1    Ibrahem, I.2    Vesely, J.3    Zhao, G.L.4    Córdova, A.5
  • 37
    • 34948875227 scopus 로고    scopus 로고
    • Hydrazide-catalyzed 1,3-dipolar nitrone cycloadditions
    • Lemay, M.; Trant, J.; Ogilvie, W. W., Hydrazide-catalyzed 1,3-dipolar nitrone cycloadditions. Tetrahedron 2007, 63 (47), 11644-11655.
    • (2007) Tetrahedron , vol.63 , Issue.47 , pp. 11644-11655
    • Lemay, M.1    Trant, J.2    Ogilvie, W.W.3
  • 38
    • 33847051178 scopus 로고    scopus 로고
    • Organocatalytic asymmetric 5-hydroxyisoxazolidine synthesis: A highly enantioselective route to beta-amino acids
    • Ibrahem, I.; Rios, R.; Vesely, J.; Zhao, G. L.; Córdova, A., Organocatalytic asymmetric 5-hydroxyisoxazolidine synthesis: A highly enantioselective route to beta-amino acids. Chem. Commun. (Cambridge, U. K.) 2007, (8), 849-851.
    • (2007) Chem. Commun. (Cambridge, U. K.) , Issue.8 , pp. 849-851
    • Ibrahem, I.1    Rios, R.2    Vesely, J.3    Zhao, G.L.4    Córdova, A.5
  • 39
    • 42049098788 scopus 로고    scopus 로고
    • Catalytic enantioselective 5-hydroxyisoxazolidine synthesis: An asymmetric entry to beta-amino acids
    • Ibrahem, I.; Rios, R.; Vesely, J.; Zhao, G. L.; Córdova, A., Catalytic enantioselective 5-hydroxyisoxazolidine synthesis: An asymmetric entry to beta-amino acids. Synthesis-Stuttgart 2008, (7), 1153-1157.
    • (2008) Synthesis-Stuttgart , Issue.7 , pp. 1153-1157
    • Ibrahem, I.1    Rios, R.2    Vesely, J.3    Zhao, G.L.4    Córdova, A.5
  • 40
    • 33845192393 scopus 로고    scopus 로고
    • A new organocatalyst for 1,3-dipolar cycloadditions of nitrones to alpha, beta - unsaturated aldehydes
    • Chow, S. S.; Nevalainen, M.; Evans, C. A.; Johannes, C. W., A new organocatalyst for 1,3-dipolar cycloadditions of nitrones to alpha, beta - unsaturated aldehydes. Tetrahedron Lett. 2006, 48 (2), 277-280.
    • (2006) Tetrahedron Lett , vol.48 , Issue.2 , pp. 277-280
    • Chow, S.S.1    Nevalainen, M.2    Evans, C.A.3    Johannes, C.W.4
  • 41
    • 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, (19), 2997-3000.
    • (2008) Synlett , Issue.19 , pp. 2997-3000
    • Du, W.1    Liu, Y.-K.2    Yue, L.3    Chen, Y.-C.4
  • 42
    • 69249089792 scopus 로고    scopus 로고
    • Hybrid diamines derived from 1,1 '-binaphthyl-2,2 '-diamine and alpha-amino acids as organocatalysts for 1,3-dipolar cycloaddition of aromatic nitrones to (E)-crotonaldehyde
    • Weselinski, L.; Stepniak, P.; Jurczak, J., Hybrid Diamines Derived from 1,1 '-Binaphthyl-2,2 '-diamine and alpha-Amino Acids as Organocatalysts for 1,3-Dipolar Cycloaddition of Aromatic Nitrones to (E)-Crotonaldehyde. Synlett 2009, (14), 2261-2264.
    • (2009) Synlett , Issue.14 , pp. 2261-2264
    • Weselinski, L.1    Stepniak, P.2    Jurczak, J.3
  • 43
    • 70349900639 scopus 로고    scopus 로고
    • Highly stereoselective one-pot synthesis of bicyclic isoxazolidines with five stereogenic centers by an organocatalytic process
    • Zhu, D.; Lu, M.; Dai, L.; Zhong, G. F., Highly Stereoselective One-Pot Synthesis of Bicyclic Isoxazolidines with Five Stereogenic Centers by an Organocatalytic Process. Angewandte Chemie-International Edition 2009, 48 (33), 6089-6092.
    • (2009) Angewandte Chemie-International Edition , vol.48 , Issue.33 , pp. 6089-6092
    • Zhu, D.1    Lu, M.2    Dai, L.3    Zhong, G.F.4
  • 44
    • 77949735799 scopus 로고    scopus 로고
    • Water-more than just a green solvent: A stereoselective one-pot access to all-chiral tetrahydronaphthalenes in aqueous media
    • Tan, B.; Zhu, D.; Zhang, L. H.; Chua, P. J.; Zeng, X. F.; Zhong, G. F., Water-More Than Just a Green Solvent: A Stereoselective One-Pot Access to All-Chiral Tetrahydronaphthalenes in Aqueous Media. Chemistry-a European Journal 2010, 16 (12), 3842-3848.
    • (2010) Chemistry-a European Journal , vol.16 , Issue.12 , pp. 3842-3848
    • Tan, B.1    Zhu, D.2    Zhang, L.H.3    Chua, P.J.4    Zeng, X.F.5    Zhong, G.F.6
  • 45
    • 33646142092 scopus 로고    scopus 로고
    • Organocatalytic direct michael reaction of ketones and aldehydes with beta -nitrostyrene in brine
    • Mase, N.; Watanabe, K.; Yoda, H.; Takabe, K.; Tanaka, F.; Barbas, C. F., III, Organocatalytic Direct Michael Reaction of Ketones and Aldehydes with beta -Nitrostyrene in Brine. J. Am. Chem. Soc. 2006, 128 (15), 4966-4967.
    • (2006) J. Am. Chem. Soc. , vol.128 , Issue.15 , pp. 4966-4967
    • Mase, N.1    Watanabe, K.2    Yoda, H.3    Takabe, K.4    Tanaka, F.5    Barbas III., C.F.6
  • 47
    • 37249032343 scopus 로고    scopus 로고
    • Enantioselective organocatalytic intramolecular aza-michael reaction: A concise synthesis of (+)-sedamine, (+)-allosedamine, and (+)-coniine
    • Fustero, S.; Jimenez, D.; Moscardo, J.; Catalan, S.; del Pozo, C., Enantioselective Organocatalytic Intramolecular Aza-Michael Reaction: a Concise Synthesis of (+)-Sedamine, (+)-Allosedamine, and (+)-Coniine. Org. Lett. 2007, 9 (25), 5283-5286.
    • (2007) Org. Lett. , vol.9 , Issue.25 , pp. 5283-5286
    • Fustero, S.1    Jimenez, D.2    Moscardo, J.3    Catalan, S.4    del Pozo, C.5
  • 48
    • 33845190114 scopus 로고    scopus 로고
    • Asymmetric synthesis of highly functionalized tetrahydrothiophenes by organocatalytic domino reactions
    • Brandau, S.; Maerten, E.; Jorgensen, K. A., Asymmetric synthesis of highly functionalized tetrahydrothiophenes by organocatalytic domino reactions. J. Am. Chem. Soc. 2006, 128 (46), 14986-14991.
    • (2006) J. Am. Chem. Soc. , vol.128 , Issue.46 , pp. 14986-14991
    • Brandau, S.1    Maerten, E.2    Jorgensen, K.A.3
  • 49
    • 34248357847 scopus 로고    scopus 로고
    • Enantioselective organocatalytic double michael addition reactions
    • Li, H.; Zu, L.; Xie, H.; Wang, J.; Jiang, W.; Wang, W., Enantioselective Organocatalytic Double Michael Addition Reactions. Org. Lett. 2007, 9 (9), 1833-1835.
    • (2007) Org. Lett. , vol.9 , Issue.9 , pp. 1833-1835
    • Li, H.1    Zu, L.2    Xie, H.3    Wang, J.4    Jiang, W.5    Wang, W.6
  • 50
    • 65349183417 scopus 로고    scopus 로고
    • Enatioselective organocatalytic synthesis of highly functionalized tetrahydrothiophenes by a Michael-aldol cascade reaction
    • Luo, G. S.; Zhang, S. L.; Duan, W. H.; Wang, W., Enatioselective organocatalytic synthesis of highly functionalized tetrahydrothiophenes by a Michael-aldol cascade reaction. Tetrahedron Lett. 2009, 50 (24), 2946-2948.
    • (2009) Tetrahedron Lett , vol.50 , Issue.24 , pp. 2946-2948
    • Luo, G.S.1    Zhang, S.L.2    Duan, W.H.3    Wang, W.4
  • 51
    • 34250002963 scopus 로고    scopus 로고
    • A highly enantioselective catalytic domino aza-Michael/aldol reaction: One-pot organocatalytic asymmetric synthesis of 1,2-dihydroquinolidines
    • Sunden, H.; Rios, R.; Ibrahem, I.; Zhao, G. L.; Eriksson, L.; Córdova, A., A highly enantioselective catalytic domino aza-Michael/aldol reaction: One-pot organocatalytic asymmetric synthesis of 1,2-dihydroquinolidines. Advanced Synthesis & Catalysis 2007, 349 (6), 827-832.
    • (2007) Advanced Synthesis & Catalysis , vol.349 , Issue.6 , pp. 827-832
    • Sunden, H.1    Rios, R.2    Ibrahem, I.3    Zhao, G.L.4    Eriksson, L.5    Córdova, A.6
  • 52
    • 33947582613 scopus 로고    scopus 로고
    • Chiral diphenylprolinol TES ether promoted conjugate addition-aldol-dehydration reactions between α,β-unsaturated aldehydes and 2-NProtected amino benzaldehydes
    • Li, H.; Wang, J.; Xie, H.; Zu, L.; Jiang, W.; Duesler, E. N.; Wang, W., Chiral Diphenylprolinol TES Ether Promoted Conjugate Addition-Aldol-dehydration Reactions between α,β-Unsaturated Aldehydes and 2-NProtected Amino Benzaldehydes. Org. Lett. 2007, 9 (6), 965-968.
    • (2007) Org. Lett. , vol.9 , Issue.6 , pp. 965-968
    • Li, H.1    Wang, J.2    Xie, H.3    Zu, L.4    Jiang, W.5    Duesler, E.N.6    Wang, W.7
  • 53
    • 57749100152 scopus 로고    scopus 로고
    • Organocatalytic asymmetric alpha-aminoxylation/Aza-Michael reactions for the synthesis of functionalized tetrahydro-1,2-oxazines
    • Lu, M.; Zhu, D.; Lu, Y. P.; Hou, Y. X.; Tan, B.; Zhong, G. F., Organocatalytic Asymmetric alpha-Aminoxylation/Aza-Michael Reactions for the Synthesis of Functionalized Tetrahydro-1,2-oxazines. Angewandte Chemie-International Edition 2008, 47 (52), 10187-10191.
    • (2008) Angewandte Chemie-International Edition , vol.47 , Issue.52 , pp. 10187-10191
    • Lu, M.1    Zhu, D.2    Lu, Y.P.3    Hou, Y.X.4    Tan, B.5    Zhong, G.F.6
  • 54
    • 55549148449 scopus 로고    scopus 로고
    • Organocatalytic approach to benzofused nitrogencontaining heterocycles: Enantioselective total synthesis of (+)-Angustureine
    • Fustero, S.; Moscardo, J.; Jimenez, D.; Peerez-Carrion, M. D.; Sanchez-Rosesllo, M.; del Pozo, C., Organocatalytic approach to benzofused nitrogencontaining heterocycles: enantioselective total synthesis of (+)-Angustureine. Chem.--Eur. J. 2008, 14 (32), 9868-9872.
    • (2008) Chem.-Eur. J. , vol.14 , Issue.32 , pp. 9868-9872
    • Fustero, S.1    Moscardo, J.2    Jimenez, D.3    Peerez-Carrion, M.D.4    Sanchez-Rosesllo, M.5    del Pozo, C.6
  • 55
    • 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 (34), 10558-10559.
    • (2004) J. Am. Chem. Soc. , vol.126 , Issue.34 , pp. 10558-10559
    • Taylor, M.S.1    Jacobsen, E.N.2
  • 56
    • 35948942795 scopus 로고    scopus 로고
    • Enantioselective pictet-spengler-type cyclizations of hydroxylactams: Hbond donor catalysis by anion binding
    • Raheem, I. T.; Thiara, P. S.; Peterson, E. A.; Jacobsen, E. N., Enantioselective pictet-spengler-type cyclizations of hydroxylactams: Hbond donor catalysis by anion binding. J. Am. Chem. Soc. 2007, 129, 13404-13406.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 13404-13406
    • Raheem, I.T.1    Thiara, P.S.2    Peterson, E.A.3    Jacobsen, E.N.4
  • 58
    • 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 (4), 1086-1087.
    • (2006) J. Am. Chem. Soc. , vol.128 , Issue.4 , pp. 1086-1087
    • Seayad, J.1    Seayad, A.M.2    List, B.3
  • 60
    • 62749185586 scopus 로고    scopus 로고
    • Weak Bronsted Acid-Thiourea Co-catalysis: Enantioselective, Catalytic Protio-Pictet-Spengler Reactions
    • Klausen, R. S.; Jacobsen, E. N., Weak Bronsted Acid-Thiourea Co-catalysis: Enantioselective, Catalytic Protio-Pictet-Spengler Reactions. Org. Lett. 2009, 11 (4), 887-890.
    • (2009) Org. Lett. , vol.11 , Issue.4 , pp. 887-890
    • Klausen, R.S.1    Jacobsen, E.N.2
  • 61
    • 25144451926 scopus 로고    scopus 로고
    • Organocatalytic diastereo- and enantioselective annulation reactions-construction of optically active 1,2-dihydroisoquinoline and 1,2-dihydrophthalazine derivatives
    • Frisch, K.; Landa, A.; Saaby, S.; Joergensen, K. A., Organocatalytic diastereo-and enantioselective annulation reactions-construction of optically active 1,2-dihydroisoquinoline and 1,2-dihydrophthalazine derivatives. Angew. Chem., Int. Ed. 2005, 44 (37), 6058-6063.
    • (2005) Angew. Chem., Int. Ed. , vol.44 , Issue.37 , pp. 6058-6063
    • Frisch, K.1    Landa, A.2    Saaby, S.3    Joergensen, K.A.4
  • 62
    • 0344927944 scopus 로고    scopus 로고
    • Proline-Catalyzed Asymmetric Addition Reaction of 9-Tosyl-3,4-dihydro-beta - carboline with Ketones
    • Itoh, T.; Yokoya, M.; Miyauchi, K.; Nagata, K.; Ohsawa, A., Proline-Catalyzed Asymmetric Addition Reaction of 9-Tosyl-3,4-dihydro-beta - carboline with Ketones. Org. Lett. 2003, 5 (23), 4301-4304.
    • (2003) Org. Lett. , vol.5 , Issue.23 , pp. 4301-4304
    • Itoh, T.1    Yokoya, M.2    Miyauchi, K.3    Nagata, K.4    Ohsawa, A.5
  • 63
    • 33646448408 scopus 로고    scopus 로고
    • Total Synthesis of ent-Dihydrocorynantheol by Using a Proline-Catalyzed Asymmetric Addition Reaction
    • Itoh, T.; Yokoya, M.; Miyauchi, K.; Nagata, K.; Ohsawa, A., Total Synthesis of ent-Dihydrocorynantheol by Using a Proline-Catalyzed Asymmetric Addition Reaction. Org. Lett. 2006, 8 (8), 1533-1535.
    • (2006) Org. Lett. , vol.8 , Issue.8 , pp. 1533-1535
    • Itoh, T.1    Yokoya, M.2    Miyauchi, K.3    Nagata, K.4    Ohsawa, A.5
  • 64
    • 2442435852 scopus 로고    scopus 로고
    • Enantioselective Tandem ONitroso Aldol/Michael Reaction
    • Yamamoto, Y.; Momiyama, N.; Yamamoto, H., Enantioselective Tandem ONitroso Aldol/Michael Reaction. J. Am. Chem. Soc. 2004, 126 (19), 5962-5963.
    • (2004) J. Am. Chem. Soc. , vol.126 , Issue.19 , pp. 5962-5963
    • Yamamoto, Y.1    Momiyama, N.2    Yamamoto, H.3
  • 65
    • 33846781519 scopus 로고    scopus 로고
    • Diastereo- and Enantioselective Synthesis of Nitroso Diels-Alder-Type Bicycloketones Using Dienamine: Mechanistic Insight into Sequential Nitroso Aldol/Michael Reaction and Application for Optically Pure 1-Amino-3,4-diol Synthesis
    • Momiyama, N.; Yamamoto, Y.; Yamamoto, H., Diastereo- and Enantioselective Synthesis of Nitroso Diels-Alder-Type Bicycloketones Using Dienamine: Mechanistic Insight into Sequential Nitroso Aldol/Michael Reaction and Application for Optically Pure 1-Amino-3,4-diol Synthesis. J. Am. Chem. Soc. 2007, 129 (5), 1190-1195.
    • (2007) J. Am. Chem. Soc. , vol.129 , Issue.5 , pp. 1190-1195
    • Momiyama, N.1    Yamamoto, Y.2    Yamamoto, H.3
  • 66
    • 23744473863 scopus 로고    scopus 로고
    • Direct catalytic enantioselective aza-Diels-Alder reactions
    • Sunden, H.; Ibrahem, I.; Eriksson, L.; Córdova, A., Direct catalytic enantioselective aza-Diels-Alder reactions. Angew. Chem., Int. Ed. 2005, 44 (31), 4877-4880.
    • (2005) Angew. Chem., Int. Ed. , vol.44 , Issue.31 , pp. 4877-4880
    • Sunden, H.1    Ibrahem, I.2    Eriksson, L.3    Córdova, A.4
  • 67
    • 33845202285 scopus 로고    scopus 로고
    • Chiral N-heterocyclic carbene catalyzed, enantioselective oxodiene Diels-Alder reactions with low catalyst loadings
    • He, M.; Uc, G. J.; Bode, J. W., Chiral N-heterocyclic carbene catalyzed, enantioselective oxodiene Diels-Alder reactions with low catalyst loadings. J. Am. Chem. Soc. 2006, 128, 15088-15089.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 15088-15089
    • He, M.1    Uc, G.J.2    Bode, J.W.3
  • 68
    • 33846157409 scopus 로고    scopus 로고
    • Enantioselective direct aza hetero-Diels-Alder reaction catalyzed by chiral Bronsted 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 Bronsted acids. Org. Lett. 2006, 8 (26), 6023-6026.
    • (2006) Org. Lett. , vol.8 , Issue.26 , pp. 6023-6026
    • Liu, H.1    Cun, L.F.2    Mi, A.Q.3    Jiang, Y.Z.4    Gong, L.Z.5
  • 69
    • 33746801098 scopus 로고    scopus 로고
    • Chiral Bronsted acid catalyzed enantioselective aza-Diels-Alder reaction of Brassard's diene with imines
    • Itoh, J.; Fuchibe, K.; Akiyama, T., Chiral Bronsted acid catalyzed enantioselective aza-Diels-Alder reaction of Brassard's diene with imines. Angewandte Chemie-International Edition 2006, 45 (29), 4796-4798.
    • (2006) Angewandte Chemie-International Edition , vol.45 , Issue.29 , pp. 4796-4798
    • Itoh, J.1    Fuchibe, K.2    Akiyama, T.3
  • 70
    • 33749522044 scopus 로고    scopus 로고
    • Chiral Bronsted Acid-Catalyzed Inverse Electron-Demand Aza Diels-Alder Reaction
    • Akiyama, T.; Morita, H.; Fuchibe, K., Chiral Bronsted Acid-Catalyzed Inverse Electron-Demand Aza Diels-Alder Reaction. J. Am. Chem. Soc. 2006, 128 (40), 13070-13071.
    • (2006) J. Am. Chem. Soc. , vol.128 , Issue.40 , pp. 13070-13071
    • Akiyama, T.1    Morita, H.2    Fuchibe, K.3
  • 71
    • 77149152524 scopus 로고    scopus 로고
    • Asymmetric Cooperative Catalysis of Strong Bronsted Acid-Promoted Reactions Using Chiral Ureas
    • Xu, H.; Zuend, S. J.; Woll, M. G.; Tao, Y.; Jacobsen, E. N., Asymmetric Cooperative Catalysis of Strong Bronsted Acid-Promoted Reactions Using Chiral Ureas. Science 2010, 327 (5968), 986-990.
    • (2010) Science , vol.327 , Issue.5968 , pp. 986-990
    • Xu, H.1    Zuend, S.J.2    Woll, M.G.3    Tao, Y.4    Jacobsen, E.N.5
  • 72
    • 57549095456 scopus 로고    scopus 로고
    • Organocatalytic asymmetric inverse-electron-demand aza-Diels-Alder reaction of N-sulfonyl- 1-aza-1,3-butadienes and aldehydes
    • Han, B.; Li, J.-L.; Ma, C.; Zhang, S.-J.; Chen, Y.-C., Organocatalytic asymmetric inverse-electron-demand aza-Diels-Alder reaction of N-sulfonyl- 1-aza-1,3-butadienes and aldehydes. Angew. Chem., Int. Ed. 2008, 47 (51), 9971-9974.
    • (2008) Angew. Chem., Int. Ed. , vol.47 , Issue.51 , pp. 9971-9974
    • Han, B.1    Li, J.-L.2    Ma, C.3    Zhang, S.-J.4    Chen, Y.-C.5
  • 73
    • 76249093698 scopus 로고    scopus 로고
    • Enantioselective construction of lactone [2,3-b]piperidine skeletons via organocatalytic tandem reactions
    • He, Z.-Q.; Han, B.; Li, R.; Wu, L.; Chen, Y.-C., Enantioselective construction of lactone [2,3-b]piperidine skeletons via organocatalytic tandem reactions. Org. Biomol. Chem. 2010, 8 (4), 755-757.
    • (2010) Org. Biomol. Chem. , vol.8 , Issue.4 , pp. 755-757
    • He, Z.-Q.1    Han, B.2    Li, R.3    Wu, L.4    Chen, Y.-C.5
  • 74
    • 70349769741 scopus 로고    scopus 로고
    • Organocatalytic Regio- and Stereoselective Inverse-Electron-Demand Aza- Diels-Alder Reaction of alpha, beta -Unsaturated Aldehydes and N-Tosyl-1- aza-1,3-butadienes
    • Han, B.; He, Z.-Q.; Li, J.-L.; Li, R.; Jiang, K.; Liu, T.-Y.; Chen, Y.-C., Organocatalytic Regio- and Stereoselective Inverse-Electron-Demand Aza-Diels-Alder Reaction of alpha, beta -Unsaturated Aldehydes and N-Tosyl-1- aza-1,3-butadienes. Angew. Chem., Int. Ed. 2009, 48 (30), 5474-5477.
    • (2009) Angew. Chem., Int. Ed. , vol.48 , Issue.30 , pp. 5474-5477
    • Han, B.1    He, Z.-Q.2    Li, J.-L.3    Li, R.4    Jiang, K.5    Liu, T.-Y.6    Chen, Y.-C.7
  • 76
    • 34548259270 scopus 로고    scopus 로고
    • Chiral Bronsted Acid-Catalyzed Tandem Aza-Ene Type Reaction/Cyclization Cascade for a One-Pot Entry to Enantioenriched Piperidines
    • Terada, M.; Machioka, K.; Sorimachi, K., Chiral Bronsted Acid-Catalyzed Tandem Aza-Ene Type Reaction/Cyclization Cascade for a One-Pot Entry to Enantioenriched Piperidines. J. Am. Chem. Soc. 2007, 129 (34), 10336-10337.
    • (2007) J. Am. Chem. Soc. , vol.129 , Issue.34 , pp. 10336-10337
    • Terada, M.1    Machioka, K.2    Sorimachi, K.3
  • 77
    • 53549111081 scopus 로고    scopus 로고
    • A highly enantioselective Bronsted acid catalyzed reaction cascade
    • Rueping, M.; Antonchick, A. P., A highly enantioselective Bronsted acid catalyzed reaction cascade. Angewandte Chemie-International Edition 2008, 47 (31), 5836-5838.
    • (2008) Angewandte Chemie-International Edition , vol.47 , Issue.31 , pp. 5836-5838
    • Rueping, M.1    Antonchick, A.P.2
  • 78
    • 58249101213 scopus 로고    scopus 로고
    • Asymmetric Alkaloid Synthesis: A One-Pot Organocatalytic Reaction to Quinolizidine Derivatives
    • Franzen, J.; Fisher, A., Asymmetric Alkaloid Synthesis: A One-Pot Organocatalytic Reaction to Quinolizidine Derivatives. Angewandte Chemie-International Edition 2009, 48 (4), 787-791.
    • (2009) Angewandte Chemie-International Edition , vol.48 , Issue.4 , pp. 787-791
    • Franzen, J.1    Fisher, A.2
  • 79
    • 77349124192 scopus 로고    scopus 로고
    • Diverse Asymmetric Quinolizidine Synthesis: A Stereodivergent One-Pot Approach
    • Zhang, W.; Franzen, J., Diverse Asymmetric Quinolizidine Synthesis: A Stereodivergent One-Pot Approach. Adv. Synth. Catal. 2010, 352 (2-3), 499-518.
    • (2010) Adv. Synth. Catal. , vol.352 , Issue.2-3 , pp. 499-518
    • Zhang, W.1    Franzen, J.2
  • 80
    • 61749096057 scopus 로고    scopus 로고
    • Highly enantioselective organocatalytic synthesis of piperidines. Formal synthesis of (-)-Paroxetine
    • Valero, G.; Schimer, J.; Cisarova, I.; Vesely, J.; Moyano, A.; Rios, R., Highly enantioselective organocatalytic synthesis of piperidines. Formal synthesis of (-)-Paroxetine. Tetrahedron Lett. 2009, 50 (17), 1943-1946.
    • (2009) Tetrahedron Lett , vol.50 , Issue.17 , pp. 1943-1946
    • Valero, G.1    Schimer, J.2    Cisarova, I.3    Vesely, J.4    Moyano, A.5    Rios, R.6
  • 81
    • 77950257271 scopus 로고    scopus 로고
    • Multiple-Organocatalyst-Promoted Cascade Reaction: A Fast and Efficient Entry into Fully Substituted Piperidines
    • Wang, Y.; Yu, D. F.; Liu, Y. Z.; Wei, H.; Luo, Y. C.; Dixon, D. J.; Xu, P. F., Multiple-Organocatalyst-Promoted Cascade Reaction: A Fast and Efficient Entry into Fully Substituted Piperidines. Chemistry-a European Journal 2010, 16 (13), 3922-3925.
    • (2010) Chemistry-a European Journal , vol.16 , Issue.13 , pp. 3922-3925
    • Wang, Y.1    Yu, D.F.2    Liu, Y.Z.3    Wei, H.4    Luo, Y.C.5    Dixon, D.J.6    Xu, P.F.7
  • 82
    • 33846250463 scopus 로고    scopus 로고
    • Catalytic enantioselective domino oxa-Michael/aldol condensations: Asymmetric synthesis of benzopyran derivatives
    • Sunden, H.; Ibrahem, I.; Zhao, G.-L.; Eriksson, L.; Córdova, A., Catalytic enantioselective domino oxa-Michael/aldol condensations: asymmetric synthesis of benzopyran derivatives. Chem.--Eur. J. 2007, 13 (2), 574-581.
    • (2007) Chem.-Eur. J. , vol.13 , Issue.2 , pp. 574-581
    • Sunden, H.1    Ibrahem, I.2    Zhao, G.-L.3    Eriksson, L.4    Córdova, A.5
  • 83
    • 85196230282 scopus 로고    scopus 로고
    • One-pot approach to chiral chromenes via enantioselective organocatalytic domino oxa-Michael-aldol reaction (vol 47, pg 507, 2007)
    • Li, H.; Wang, J.; E-Nunu, T.; Zu, L. S.; Jiang, W.; Wei, S. H.; Wang, W., One-pot approach to chiral chromenes via enantioselective organocatalytic domino oxa-Michael-aldol reaction (vol 47, pg 507, 2007). Chem. Commun. (Cambridge, U. K.) 2007, (8), 878-878.
    • (2007) Chem. Commun. (Cambridge, U. K.) , Issue.8 , pp. 878-878
    • Li, H.1    Wang, J.2    E-Nunu, T.3    Zu, L.S.4    Jiang, W.5    Wei, S.H.6    Wang, W.7
  • 84
    • 70350022768 scopus 로고    scopus 로고
    • Chiral amine/chiral acid as an excellent organocatalytic system for the enantioselective tandem oxa-Michael-aldol reaction
    • Luo, S. P.; Li, Z. B.; Wang, L. P.; Guo, Y.; Xia, A. B.; Xu, D. Q., Chiral amine/chiral acid as an excellent organocatalytic system for the enantioselective tandem oxa-Michael-aldol reaction. Org. Biomol. Chem. 2009, 7 (21), 4539-4546.
    • (2009) Org. Biomol. Chem , vol.7 , Issue.21 , pp. 4539-4546
    • Luo, S.P.1    Li, Z.B.2    Wang, L.P.3    Guo, Y.4    Xia, A.B.5    Xu, D.Q.6
  • 85
    • 33847068325 scopus 로고    scopus 로고
    • A simple and concise catalytic asymmetric entry to tetrahydroxanthenones
    • Rios, R.; Sunden, H.; Ibrahem, I.; Córdova, A., A simple and concise catalytic asymmetric entry to tetrahydroxanthenones. Tetrahedron Lett. 2007, 48 (12), 2181-2184.
    • (2007) Tetrahedron Lett , vol.48 , Issue.12 , pp. 2181-2184
    • Rios, R.1    Sunden, H.2    Ibrahem, I.3    Córdova, A.4
  • 86
    • 75249100345 scopus 로고    scopus 로고
    • Dual Organocatalytic Ion-Pair Assemblies: A Highly Efficient Approach for the Enantioselective Oxa-Michael-Mannich Reaction of Salicylic Aldehydes with Cyclohexenones
    • Xia, A. B.; Xu, D. Q.; Luo, S. P.; Jiang, J. R.; Tang, J.; Wang, Y. F.; Xu, Z. Y., Dual Organocatalytic Ion-Pair Assemblies: A Highly Efficient Approach for the Enantioselective Oxa-Michael-Mannich Reaction of Salicylic Aldehydes with Cyclohexenones. Chemistry-a European Journal 2010, 16 (3), 801-804.
    • (2010) Chemistry-a European Journal , vol.16 , Issue.3 , pp. 801-804
    • Xia, A.B.1    Xu, D.Q.2    Luo, S.P.3    Jiang, J.R.4    Tang, J.5    Wang, Y.F.6    Xu, Z.Y.7
  • 87
    • 56649105308 scopus 로고    scopus 로고
    • A novel enantioselective catalytic tandem oxa-Michael-Henry reaction: One-pot organocatalytic asymmetric synthesis of 3-nitro-2Hchromenes
    • Xu, D.-Q.; Wang, Y.-F.; Luo, S.-P.; Zhang, S.; Zhong, A.-G.; Chen, H.; Xu, Z.-Y., A novel enantioselective catalytic tandem oxa-Michael-Henry reaction: one-pot organocatalytic asymmetric synthesis of 3-nitro-2Hchromenes. Adv. Synth. Catal. 2008, 350 (16), 2610-2616.
    • (2008) Adv. Synth. Catal. , vol.350 , Issue.16 , pp. 2610-2616
    • Xu, D.-Q.1    Wang, Y.-F.2    Luo, S.-P.3    Zhang, S.4    Zhong, A.-G.5    Chen, H.6    Xu, Z.-Y.7
  • 88
    • 76649129328 scopus 로고    scopus 로고
    • Iminium-Allenamine Cascade Catalysis: One-Pot Access to Chiral 4H-Chromenes by a Highly Enantioselective Michael-Michael Sequence
    • Zhang, X. S.; Zhang, S. L.; Wang, W., Iminium-Allenamine Cascade Catalysis: One-Pot Access to Chiral 4H-Chromenes by a Highly Enantioselective Michael-Michael Sequence. Angewandte Chemie-International Edition 2010, 49 (8), 1481-1484.
    • (2010) Angewandte Chemie-International Edition , vol.49 , Issue.8 , pp. 1481-1484
    • Zhang, X.S.1    Zhang, S.L.2    Wang, W.3
  • 89
    • 0242432417 scopus 로고    scopus 로고
    • Hydrogen bonding: Single enantiomers from a chiral-alcohol catalyst
    • Huang, Y.; Unni, A. K.; Thadani, A. N.; Rawal, V. H., Hydrogen bonding: Single enantiomers from a chiral-alcohol catalyst. Nature 2003, 424 (6945), 146-146.
    • (2003) Nature , vol.424 , Issue.6945 , pp. 146-146
    • Huang, Y.1    Unni, A.K.2    Thadani, A.N.3    Rawal, V.H.4
  • 90
    • 13444265956 scopus 로고    scopus 로고
    • Axially chiral biaryl diols catalyze highly enantioselective hetero-Diels-Alder reactions through hydrogen bonding
    • Unni, A. K.; Takenaka, N.; Yamamoto, H.; Rawal, V. H., Axially chiral biaryl diols catalyze highly enantioselective hetero-Diels-Alder reactions through hydrogen bonding. J. Am. Chem. Soc. 2005, 127 (5), 1336-1337.
    • (2005) J. Am. Chem. Soc. , vol.127 , Issue.5 , pp. 1336-1337
    • Unni, A.K.1    Takenaka, N.2    Yamamoto, H.3    Rawal, V.H.4
  • 91
    • 0344835672 scopus 로고    scopus 로고
    • The first organocatalytic enantioselective inverseelectron-demand hetero-Diels-Alder reaction
    • Juhl, K.; Jorgensen, K. A., The first organocatalytic enantioselective inverseelectron-demand hetero-Diels-Alder reaction. Angew. Chem., Int. Ed. 2003, 42 (13), 1498-1501.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , Issue.13 , pp. 1498-1501
    • Juhl, K.1    Jorgensen, K.A.2
  • 92
    • 34547402618 scopus 로고    scopus 로고
    • Inverse-electron-demand hetero-Diels-Alder reaction of beta,gamma-unsaturated alphaketophosphonates catalyzed by prolinal dithioacetals
    • Samanta, S.; Krause, J.; Mandal, T.; Zhao, C. G., Inverse-electron-demand hetero-Diels-Alder reaction of beta,gamma-unsaturated alphaketophosphonates catalyzed by prolinal dithioacetals. Org. Lett. 2007, 9 (14), 2745-2748.
    • (2007) Org. Lett. , vol.9 , Issue.14 , pp. 2745-2748
    • Samanta, S.1    Krause, J.2    Mandal, T.3    Zhao, C.G.4
  • 93
    • 42949123558 scopus 로고    scopus 로고
    • Organocatalyzed asymmetric inverseelectron-demand hetero-Diels-Alder reaction of alpha, beta -unsaturated trifluoromethyl ketones and aldehydes
    • Zhao, Y.; Wang, X.-J.; Liu, J.-T., Organocatalyzed asymmetric inverseelectron-demand hetero-Diels-Alder reaction of alpha, beta -unsaturated trifluoromethyl ketones and aldehydes. Synlett 2008, (7), 1017-1020.
    • (2008) Synlett , Issue.7 , pp. 1017-1020
    • Zhao, Y.1    Wang, X.-J.2    Liu, J.-T.3
  • 94
    • 55949132381 scopus 로고    scopus 로고
    • Chiral NHC-catalyzed oxodiene Diels-Alder reactions with alpha-chloroaldehyde bisulfite salts
    • He, M.; Beahm, B. J.; Bode, J. W., Chiral NHC-catalyzed oxodiene Diels-Alder reactions with alpha-chloroaldehyde bisulfite salts. Org. Lett. 2008, 10 (17), 3817-3820.
    • (2008) Org. Lett. , vol.10 , Issue.17 , pp. 3817-3820
    • He, M.1    Beahm, B.J.2    Bode, J.W.3
  • 95
    • 77954281480 scopus 로고    scopus 로고
    • An enantioselective claisen rearrangement catalyzed by N-Heterocyclic carbenes
    • Kaeobamrung, J.; Mahatthananchai, J.; Zheng, P.; Bode, J. W., An Enantioselective Claisen Rearrangement Catalyzed by N-Heterocyclic Carbenes. J. Am. Chem. Soc. 2010, 132 (26), 8810-8812.
    • (2010) J. Am. Chem. Soc. , vol.132 , Issue.26 , pp. 8810-8812
    • Kaeobamrung, J.1    Mahatthananchai, J.2    Zheng, P.3    Bode, J.W.4
  • 96
    • 33846367349 scopus 로고    scopus 로고
    • Enantioselective synthesis of 3,4-dihydropyran-2-ones by domino Michael addition and lactonization with new asymmetric organocatalysts: Cinchona-alkaloidderived chiral quaternary ammonium phenoxides
    • Tozawa, T.; Nagao, H.; Yamane, Y.; Mukaiyama, T., Enantioselective synthesis of 3,4-dihydropyran-2-ones by domino Michael addition and lactonization with new asymmetric organocatalysts: Cinchona-alkaloidderived chiral quaternary ammonium phenoxides. Chemistry-an Asian Journal 2007, 2 (1), 123-134.
    • (2007) Chemistry-an Asian Journal , vol.2 , Issue.1 , pp. 123-134
    • Tozawa, T.1    Nagao, H.2    Yamane, Y.3    Mukaiyama, T.4
  • 97
    • 53549126884 scopus 로고    scopus 로고
    • Asymmetric iminium ion catalysis: An efficient enantioselective synthesis of pyranonaphthoquinones and betalapachones
    • Rueping, M.; Sugiono, E.; Merino, E., Asymmetric iminium ion catalysis: An efficient enantioselective synthesis of pyranonaphthoquinones and betalapachones. Angewandte Chemie-International Edition 2008, 47 (16), 3046-3049.
    • (2008) Angewandte Chemie-International Edition , vol.47 , Issue.16 , pp. 3046-3049
    • Rueping, M.1    Sugiono, E.2    Merino, E.3
  • 98
    • 53849116779 scopus 로고    scopus 로고
    • Asymmetric organocatalysis: An efficient enantioselective access to benzopyrans and chromenes
    • Rueping, M.; Sugiono, E.; Merino, E., Asymmetric organocatalysis: an efficient enantioselective access to benzopyrans and chromenes. Chem.--Eur. J. 2008, 14 (21), 6329-6332.
    • (2008) Chem.-Eur. J. , vol.14 , Issue.21 , pp. 6329-6332
    • Rueping, M.1    Sugiono, E.2    Merino, E.3
  • 99
    • 69549126459 scopus 로고    scopus 로고
    • Organocatalytic asymmetric friedel-crafts alkylation/cyclization cascade reaction of 1- naphthols and alpha, beta -unsaturated aldehydes: An enantioselective synthesis of chromanes and dihydrobenzopyranes
    • Hong, L.; Wang, L.; Sun, W.; Wong, K.; Wang, R., Organocatalytic Asymmetric Friedel-Crafts Alkylation/Cyclization Cascade Reaction of 1- Naphthols and alpha, beta -Unsaturated Aldehydes: An Enantioselective Synthesis of Chromanes and Dihydrobenzopyranes. J. Org. Chem. 2009, 74 (17), 6881-6884.
    • (2009) J. Org. Chem. , vol.74 , Issue.17 , pp. 6881-6884
    • Hong, L.1    Wang, L.2    Sun, W.3    Wong, K.4    Wang, R.5
  • 100
    • 45849136024 scopus 로고    scopus 로고
    • Proline-mediated enantioselective construction of tetrahydropyrans via a domino aidol/acetalization reaction
    • Hazelard, D.; Ishikawa, H.; Hashizume, D.; Koshino, H.; Hayashi, Y., Proline-mediated enantioselective construction of tetrahydropyrans via a domino aidol/acetalization reaction. Org. Lett. 2008, 10 (7), 1445-1448.
    • (2008) Org. Lett. , vol.10 , Issue.7 , pp. 1445-1448
    • Hazelard, D.1    Ishikawa, H.2    Hashizume, D.3    Koshino, H.4    Hayashi, Y.5
  • 101
    • 70349153511 scopus 로고    scopus 로고
    • Diphenylprolinol silyl ether as a catalyst in an asymmetric, catalytic, and direct michael reaction of nitroethanol with alpha,beta-unsaturated aldehydes
    • Gotoh, H.; Okamura, D.; Ishikawa, H.; Hayashi, Y., Diphenylprolinol Silyl Ether as a Catalyst in an Asymmetric, Catalytic, and Direct Michael Reaction of Nitroethanol with alpha,beta-Unsaturated Aldehydes. Org. Lett. 2009, 11 (18), 4056-4059.
    • (2009) Org. Lett. , vol.11 , Issue.18 , pp. 4056-4059
    • Gotoh, H.1    Okamura, D.2    Ishikawa, H.3    Hayashi, Y.4
  • 102
    • 33747594792 scopus 로고    scopus 로고
    • Enantioselective organocatalytic tandem michael-aldol reactions: One-Pot synthesis of chiral thiochromenes
    • Wang, W.; Li, H.; Wang, J.; Zu, L., Enantioselective Organocatalytic Tandem Michael-Aldol Reactions: One-Pot Synthesis of Chiral Thiochromenes. J. Am. Chem. Soc. 2006, 128 (32), 10354-10355.
    • (2006) J. Am. Chem. Soc. , vol.128 , Issue.32 , pp. 10354-10355
    • Wang, W.1    Li, H.2    Wang, J.3    Zu, L.4
  • 103
    • 33750307526 scopus 로고    scopus 로고
    • Highly enantioselective synthesis of 2H-1-benzothiopyrans by a catalytic domino reaction
    • Rios, R.; Sunden, H.; Ibrahem, I.; Zhao, G. L.; Eriksson, L.; Córdova, A., Highly enantioselective synthesis of 2H-1-benzothiopyrans by a catalytic domino reaction. Tetrahedron Lett. 2006, 47 (48), 8547-8551.
    • (2006) Tetrahedron Lett , vol.47 , Issue.48 , pp. 8547-8551
    • Rios, R.1    Sunden, H.2    Ibrahem, I.3    Zhao, G.L.4    Eriksson, L.5    Córdova, A.6
  • 104
    • 33750471190 scopus 로고    scopus 로고
    • A one-pot organocatalytic asymmetric entry to tetrahydrothioxanthenones
    • Rios, R.; Sunden, H.; Ibrahem, I.; Zhao, G. L.; Córdova, A., A one-pot organocatalytic asymmetric entry to tetrahydrothioxanthenones. Tetrahedron Lett. 2006, 47 (49), 8679-8682.
    • (2006) Tetrahedron Lett , vol.47 , Issue.49 , pp. 8679-8682
    • Rios, R.1    Sunden, H.2    Ibrahem, I.3    Zhao, G.L.4    Córdova, A.5
  • 105
    • 38849113311 scopus 로고    scopus 로고
    • Highly diastereo- and enantioselective catalytic domino thia-Michael/aldol reactions: Synthesis of benzothiopyrans with three contiguous stereocenters
    • Zhao, G.-L.; Vesely, J.; Rios, R.; Ibrahem, I.; Sunden, H.; Córdova, A., Highly diastereo- and enantioselective catalytic domino thia-Michael/aldol reactions: synthesis of benzothiopyrans with three contiguous stereocenters. Adv. Synth. Catal. 2008, 350 (2), 237-242.
    • (2008) Adv. Synth. Catal. , vol.350 , Issue.2 , pp. 237-242
    • Zhao, G.-L.1    Vesely, J.2    Rios, R.3    Ibrahem, I.4    Sunden, H.5    Córdova, A.6
  • 106
    • 47949088604 scopus 로고    scopus 로고
    • Synthesis of 2,3,4-trisubstituted thiochromanes using an organocatalytic enantioselective tandem Michael-Henry reaction
    • Dodda, R.; Goldman, J. J.; Mandal, T.; Zhao, C. G.; Broker, G. A.; Tiekink, E. R. T., Synthesis of 2,3,4-trisubstituted thiochromanes using an organocatalytic enantioselective tandem Michael-Henry reaction. Adv. Synth. Catal. 2008, 350 (4), 537-541.
    • (2008) Adv. Synth. Catal. , vol.350 , Issue.4 , pp. 537-541
    • Dodda, R.1    Goldman, J.J.2    Mandal, T.3    Zhao, C.G.4    Broker, G.A.5    Tiekink, E.R.T.6
  • 107
    • 53549133989 scopus 로고    scopus 로고
    • A highly stereoselective hydrogen-bond-mediated Michael-Michael cascade process through dynamic kinetic resolution
    • Wang, J.; Xie, H. X.; Li, H.; Zu, L. S.; Wang, W., A highly stereoselective hydrogen-bond-mediated Michael-Michael cascade process through dynamic kinetic resolution. Angewandte Chemie-International Edition 2008, 47 (22), 4177-4179.
    • (2008) Angewandte Chemie-International Edition , vol.47 , Issue.22 , pp. 4177-4179
    • Wang, J.1    Xie, H.X.2    Li, H.3    Zu, L.S.4    Wang, W.5
  • 108
    • 33846783029 scopus 로고    scopus 로고
    • Cascade Michael-Aldol reactions promoted by hydrogen bonding mediated catalysis
    • Zu, L. S.; Wang, J.; Li, H.; Xie, H. X.; Jiang, W.; Wang, W., Cascade Michael-Aldol reactions promoted by hydrogen bonding mediated catalysis. J. Am. Chem. Soc. 2007, 129, 1036-1037.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 1036-1037
    • Zu, L.S.1    Wang, J.2    Li, H.3    Xie, H.X.4    Jiang, W.5    Wang, W.6
  • 109
    • 34548388318 scopus 로고    scopus 로고
    • Chiral amine thiourea-promoted enantioselective domino Michael-aldol reactions between 2-mercaptobenzaldehydes and maleimides
    • Zu, L.; Xie, H.; Li, H.; Wang, J.; Jiang, W.; Wang, W., Chiral amine thiourea-promoted enantioselective domino Michael-aldol reactions between 2-mercaptobenzaldehydes and maleimides. Adv. Synth. Catal. 2007, 349 (11+12), 1882-1886.
    • (2007) Adv. Synth. Catal. , vol.349 , Issue.11-12 , pp. 1882-1886
    • Zu, L.1    Xie, H.2    Li, H.3    Wang, J.4    Jiang, W.5    Wang, W.6


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