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Volumn 8, Issue 24, 2002, Pages 5652-5661

Nucleophilic addition of nitrones to ketones: Development of a new catalytic asymmetric nitrone-aldol reaction

Author keywords

Aldol reaction; Amines; Asymmetric catalysis; Enantioselectivity; Nitrones

Indexed keywords

ADDITION REACTIONS; AMINES; CARBONYLATION; CATALYSIS;

EID: 0037122183     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3765(20021216)8:24<5652::AID-CHEM5652>3.0.CO;2-J     Document Type: Article
Times cited : (50)

References (62)
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    • List, B.1    Notz, W.2
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    • 0037059471 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
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    • Cordova, A.1    Notz, W.2    Barbas C.F. III3
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    • 0034812506 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5260
    • Sakthivel, K.1    Notz, W.2    Bui, T.3    Barbas C.F. III4
  • 27
    • 0035932079 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2001) Org. Lett. , vol.3 , pp. 573
    • List, B.1    Pojarliev, P.2    Castello, C.3
  • 28
    • 0034654216 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 2395
    • List, B.1    Lerner, R.A.2    Barbas C.F. III3
  • 29
    • 0002462320 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) Chem. Commun. , pp. 620
    • Bøgevig, A.1    Kumaragurubaran, N.2    Jørgensen, K.A.3
  • 30
    • 0037134880 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 6798
    • Northrup, A.B.1    MacMillan, D.W.C.2
  • 31
    • 0035825097 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 199
    • Notz, W.1    Sakthivel, K.2    Bui, T.3    Zhong, G.4    Barbas C.F. III5
  • 32
    • 0037028550 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 827
    • List, B.1    Pojarliev, P.2    Biller, W.T.3    Martin, H.J.4
  • 33
    • 0034721440 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9336
    • List, B.1
  • 34
    • 0037028990 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 1866
    • Cordova, A.1    Watanabe, S.2    Tanaka, F.3    Notz, W.4    Barbas C.F. III5
  • 35
    • 0037028924 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 1842
    • Cordova, A.1    Notz, W.2    Zhong, G.3    Betancort, J.M.4    Barbas C.F. III5
  • 36
    • 0034596452 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 6951
    • Bui, T.1    Barbas C.F. III2
  • 37
    • 0037744752 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) Angew. Chem. , vol.114 , pp. 1868
    • Bøgevig, A.1    Juhl, K.2    Kumaragubaran, N.3    Zhuang, W.4    Jørgensen, K.A.5
  • 38
    • 0347574902 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) Angew. Chem. Int. Ed. , vol.45 , pp. 1790
  • 39
    • 0037157154 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 5656
    • List, B.1
  • 40
    • 0037024190 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 6254
    • Kumaragubaran, N.1    Juhl, K.2    Zhuang, W.3    Bøgevig, A.4    Jørgensen, K.A.5
  • 41
    • 0035891780 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2001) Org. Lett. , vol.3 , pp. 3737
    • Betancort, J.M.1    Barbas C.F. III2
  • 42
    • 0035796953 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 4441
    • Betancort, J.M.1    Sakthivel, K.2    Thayumanavan, R.3    Barbas C.F. III4
  • 43
    • 0034600250 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 4243
    • Ahrendt, K.A.1    Borths, C.J.2    MacMillan, D.W.C.3
  • 44
    • 0037139610 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 2458
    • Northrup, A.B.1    MacMillan, D.W.C.2
  • 45
    • 0034638388 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9874
    • Jen, W.S.1    Wiener, J.J.M.2    MacMillan, D.W.C.3
  • 46
    • 0037166699 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) Tetrahedron Asymmetry , vol.13 , pp. 923
    • Karlsson, S.1    Högsberg, H.-E.2
  • 47
    • 0034807741 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 4370
    • Paras, N.A.1    MacMillan, D.W.C.2
  • 48
    • 0037138701 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 1172
    • Austin, J.F.1    MacMillan, D.W.C.2
  • 49
    • 0000497004 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2000) Org. Lett. , vol.2 , pp. 2975
    • Pham, V.1    Hanessian, S.2
  • 50
    • 0000902952 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2000) Angew. Chem. , vol.112 , pp. 3781
    • Horstmann, T.E.1    Guerin, D.J.2    Miller, S.J.3
  • 51
    • 0034675660 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3635
  • 52
    • 0033520752 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 10219
    • Iwabuchi, Y.1    Nakatani, M.2    Yokoyama, N.3    Hatakeyama, S.4
  • 53
    • 0037043180 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2002) Tetrahedron , vol.58 , pp. 5573
    • List, B.1
  • 54
    • 0001374973 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2001) Angew. Chem. , vol.113 , pp. 545
    • Gröger, H.1    Wilken, J.2
  • 55
    • 0346313801 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2001) Angew. Chem. Int. Ed. , vol.44 , pp. 529
  • 56
    • 0001644556 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2001) Angew. Chem. , vol.113 , pp. 3840
    • Dalko, P.I.1    Moisan, L.2
  • 57
    • 0348204618 scopus 로고    scopus 로고
    • For selected recent developments in organo-catalyzed reactions see: aldol reactions: a) B. List, W. Notz, J. Am. Chem. Soc. 2000, 122, 7386; b) A. Cordova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; c) K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; e) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; f) A. Bøgevig, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; g) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; Mannich reactions: h) W. Notz, K. Sakthivel, T. Bui, G. Zhong, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 199; i) B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827; j) B. List, J. Am. Chem. Soc. 2000, 122, 9336; k) A. Cordova, S. Watanabe, F. Tanaka, W. Notz, C. F. Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866; l) A. Cordova, W. Notz, G. Zhong, J. M. Betancort, C. F. Barbas III, J. Am. Chem. Soc. 2002, 124, 1842; Robinson annulation reactions: m) T. Bui, C. F. Barbas III, Tetrahedron Lett. 2000, 41, 6951; aminations reactions: n) A. Bøgevig, K. Juhl, N. Kumaragubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 45, 1790; o) B. List, J. Am. Chem. Soc. 2002, 124, 5656; p) N. Kumaragubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; Michael addition reactions: q) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; r) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; Diels-Alder reactions: s) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; t) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; 1,3-dipolar cycloaddition reactions: u) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; v) S. Karlsson, H.-E. Högsberg, Tetrahedron: Asymmetry 2002, 13, 923; Friedel-Crafts rections: w) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; x) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; conjugate additions: y) V. Pham, S. Hanessian, Org. Lett. 2000, 2, 2975; z) T. E. Horstmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; Baylis-Hillmann reactions: aa) Y. Iwabuchi, M. Nakatani, N. Yokoyama, S. Hatakeyama, J. Am. Chem. Soc. 1999, 121, 10219; ab) B. List, Tetrahedron 2002, 58, 5573; ac) H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545; Angew. Chem. Int. Ed. 2001, 44, 529; ad) P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840; Angew. Chem. Int. Ed. 2001, 44, 3726.
    • (2001) Angew. Chem. Int. Ed. , vol.44 , pp. 3726
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