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Volumn 43, Issue 47, 2004, Pages 6528-6531

Direct catalytic enantioselective α-aminomethylation of ketones

Author keywords

Amino alcohols; Asymmetric catalysis; Ketones; Mannich reaction

Indexed keywords

ALCOHOLS; AMINO ACIDS; CHEMICAL REACTIONS; KETONES; SYNTHESIS (CHEMICAL);

EID: 11144333506     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200460678     Document Type: Article
Times cited : (150)

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    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
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    • List, B.1    Lerner, R.A.2    Barbas III, C.F.3
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    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
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    • Notz, W.1    List, B.2
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    • 0034812506 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5260
    • Saktihvel, K.1    Notz, W.2    Bui, T.3    Barbas III, C.F.4
  • 51
    • 0037059471 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) J. Org. Chem. , vol.67 , pp. 301
    • Córdova, A.1    Notz, W.2    Barbas III, C.F.3
  • 52
    • 0035932079 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2001) Org. Lett. , vol.3 , pp. 573
    • List, B.1    Pojarliev, P.2    Castello, C.3
  • 53
    • 4243059939 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) Chem. Commun. , vol.67 , pp. 3034
    • Córdova, A.1    Notz, W.2    Barbas III, C.F.3
  • 54
    • 0002462320 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) Chem. Commun. , pp. 620
    • Bøgevig, A.1    Juhl, K.2    Kumaragurubaran, N.3    Jørgensen, K.A.4
  • 55
    • 0037134880 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 6798
    • Northrup, A.B.1    MacMillan, D.W.C.2
  • 56
    • 0037164621 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 9591
    • Chowdari, N.S.1    Ramachary, D.B.2    Córdova, A.3    Barbas III, C.F.4
  • 57
    • 4544388337 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) Angew. Chem. , vol.115 , pp. 2797
    • Pidathala, C.1    Hoang, L.2    Vignola, N.3    List, B.4
  • 58
    • 0038729533 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 2785
  • 59
    • 0037955602 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 5262
    • Tang, Z.1    Jiang, F.2    Yu, L.-T.3    Cui, X.4    Gong, L.-Z.5    Mi, A.-Q.6    Jiang, Y.-Z.7    Wu, Y.-D.8
  • 60
    • 0037744752 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) Angew. Chem. , vol.114 , pp. 1868
    • Bøgevig, A.1    Juhl, K.2    Kumaragurubaran, N.3    Zhuang, W.4    Jørgensen, K.A.5
  • 61
    • 0036260164 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1790
  • 62
    • 0037157154 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 5656
    • List, B.1
  • 63
    • 0037024190 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 6254
    • Kumaragurubaran, N.1    Juhl, K.2    Zhuang, W.3    Bøgevig, A.4    Jørgensen, K.A.5
  • 64
    • 4243062141 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2004) Angew. Chem. , vol.116 , pp. 1129
    • Bøgevig, A.1    Sundén, H.2    Córdova, A.3
  • 65
    • 1842792133 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 1109
  • 66
    • 4243085199 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2004) Angew. Chem. , vol.116 , pp. 1132
    • Hayashi, M.1    Yamaguchi, J.2    Sumaiya, T.3    Shoji, M.4
  • 67
    • 4243057730 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 1112
  • 68
    • 0842343649 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) Angew. Chem. , vol.115 , pp. 4379
    • Zhong, G.1
  • 69
    • 0141522552 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 4247
  • 70
    • 0041733541 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 10808
    • Brown, S.P.1    Brochu, M.P.2    Sinz, C.J.3    MacMillan, D.W.C.4
  • 71
    • 0000761777 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2001) Org. Lett. , vol.3 , pp. 2423
    • List, B.1    Pojarliev, P.2    Martin, H.J.3
  • 72
    • 0000497004 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2000) Org. Lett. , vol.2 , pp. 2975
    • Hanessian, S.1    Pham, V.2
  • 73
    • 0035796953 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 4441
    • Betancort, J.M.1    Sakthivel, K.2    Thayumanavan, R.3    Barbas III, C.F.4
  • 74
    • 0035891780 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2001) Org. Lett. , vol.3 , pp. 3737
    • Betancort, J.M.1    Barbas III, C.F.2
  • 75
    • 0000902952 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2000) Angew. Chem. , vol.112 , pp. 3781
    • Hortsmann, D.J.1    Guerin, D.J.2    Miller, S.J.3
  • 76
    • 0034675660 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3635
  • 77
    • 0000220483 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu,
    • (2002) Org. Lett. , vol.4 , pp. 3611
    • Alexakis, A.1    Andrey, O.2
  • 78
    • 0037070622 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 2134
    • Guerin, D.J.1    Miller, S.J.2
  • 79
    • 0013144803 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) Angew. Chem. , vol.115 , pp. 685
    • Halland, N.1    Aburel, P.S.2    Jørgensen, K.A.3
  • 80
    • 0037429423 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 661
  • 81
    • 0037195702 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) J. Org. Chem. , vol.67 , pp. 8331
    • Halland, N.1    Hazell, R.G.2    Jørgensen, K.A.3
  • 82
    • 0141563562 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) Org. Lett. , vol.5 , pp. 2559
    • Andrey, O.1    Alexakis, A.2    Bernardinelli, G.3
  • 83
    • 11144335657 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) Synlett , vol.26
    • Enders, D.1    Seki, A.2
  • 84
    • 0037139610 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 2458
    • Northrup, A.B.1    MacMillan, D.W.C.2
  • 85
    • 0034600250 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 4243
    • Ahrendt, K.A.1    Borths, C.J.2    MacMillan, D.W.C.3
  • 86
    • 0041525915 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) Angew. Chem. , vol.115 , pp. 1536
    • Juhl, K.1    Jørgensen, K.A.2
  • 87
    • 0344835672 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 1498
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    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) Nature , vol.424 , pp. 146
    • Huang, Y.1    Unni, K.2    Thadani, A.N.3    Rawal, V.H.4
  • 89
    • 0034807741 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 4370
    • Paras, N.A.1    MacMillan, D.W.C.2
  • 90
    • 0037138701 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 1172
    • Austin, J.F.1    MacMillan, D.W.C.2
  • 91
    • 0037055106 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
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    • Paras, N.A.1    MacMillan, D.W.C.2
  • 92
    • 0034638388 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9874
    • Jen, W.S.1    Wiener, J.J.M.2    MacMillan, D.W.C.3
  • 93
    • 0037166699 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003,
    • (2002) Tetrahedron: Asymmetry , vol.13 , pp. 923
    • Karlsson, S.1    Högberg, H.2
  • 94
    • 0034674972 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2000) J. Am. Chem. Soc. , vol.121 , pp. 7831
    • Taggi, A.E.1    Hafez, A.M.2    Wack, H.3    Young, B.4    Drury III, W.J.5    Lectka, T.6
  • 95
    • 0037010024 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11653
    • Sculimbrene, B.R.1    Morgan, A.J.2    Miller, S.J.3
  • 96
    • 0037467053 scopus 로고    scopus 로고
    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 2058
    • Harmata, M.1    Ghosh, S.K.2    Hong, X.3    Wacharasindhu, S.4    Kirchhoefer, P.5
  • 97
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    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
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    • Bremeyer, N.1    Smith, S.C.2    Ley, S.V.3    Gaunt, M.J.4
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    • Aldol reactions see: a) B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395; b) W. Notz, B. List, J. Am. Chem. Soc. 2000, 122, 7386; c) K. Saktihvel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260; d) A. Córdova, W. Notz, C. F. Barbas III, J. Org. Chem. 2002, 67, 301; e) B. List, P. Pojarliev, C. Castello, Org. Lett. 2001, 3, 573; f) A. Córdova, W. Notz, C. F. Barbas III, Chem. Commun. 2002, 67, 3034; g) A. Bøgevig, K. Juhl, N. Kumaragurubaran, K. A. Jørgensen, Chem. Commun. 2002, 620; h) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 6798; i) N. S. Chowdari, D. B. Ramachary, A. Córdova, C. F. Barbas III, Tetrahedron Lett. 2002, 43, 9591; j) C. Pidathala, L. Hoang, N. Vignola, B. List, Angew. Chem. 2003, 115, 2797; Angew. Chem. Int. Ed. 2003, 42, 2785; k) Z. Tang, F. Jiang, L.-T. Yu, X. Cui, L.-Z. Gong, A.-Q. Mi, Y.-Z. Jiang, Y.-D. Wu, J. Am. Chem. Soc. 2003, 125, 5262; α-Aminations see: a) A. Bøgevig, K. Juhl, N. Kumaragurubaran, W. Zhuang, K. A. Jørgensen, Angew. Chem. 2002, 114, 1868; Angew. Chem. Int. Ed. 2002, 41, 1790; b) B. List, J. Am. Chem. Soc. 2002, 124, 5656; c) N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254; α-Oxidations see: a) A. Bøgevig, H. Sundén, A. Córdova, Angew. Chem. 2004, 116, 1129; Angew. Chem. Int. Ed. 2004, 43, 1109; b) M. Hayashi, J. Yamaguchi, T. Sumaiya, M. Shoji, Angew. Chem. 2004, 116, 1132; Angew. Chem. Int. Ed. 2004, 43, 1112; c) G. Zhong, Angew. Chem. 2003, 115, 4379; Angew. Chem. Int. Ed. 2003, 42, 4247; d) S. P. Brown, M. P. Brochu, C. J. Sinz, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 10808; Michael reactions see: a) B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423; b) S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975; c) J. M. Betancort, K. Sakthivel, R. Thayumanavan, C. F. Barbas III, Tetrahedron Lett. 2001, 42, 4441; d) J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737; e) D. J. Hortsmann, D. J. Guerin, S. J. Miller, Angew. Chem. 2000, 112, 3781; Angew. Chem. Int. Ed. 2000, 39, 3635; f) A. Alexakis, O. Andrey, Org. Lett. 2002, 4, 3611; g) D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; h) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685, Angew. Chem. Int. Ed. 2003, 42, 661; i) N. Halland, R. G. Hazell, K. A. Jørgensen, J. Org. Chem. 2002, 67, 8331; j) O. Andrey, A. Alexakis, G. Bernardinelli, Org. Lett. 2003, 5, 2559; k) D. Enders, A. Seki, Synlett 2002, 26; Diels-Alder reactions see: a) A. B. Northrup, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 2458; b) K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243; hetero-Diels-Alder reactions see: a) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536; Angew. Chem. Int. Ed. 2003, 42, 1498; b) Y. Huang, K. Unni, A. N. Thadani, V. H. Rawal, Nature 2003, 424, 146; alkylation of electron-rich benzene systems see: a) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2001, 123, 4370; b) J. F. Austin, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 1172; c) N. A. Paras, D. W. C. MacMillan, J. Am. Chem. Soc. 2002, 124, 7894; 1,3-dipolar cycloadditions see: a) W. S. Jen, J. J. M. Wiener, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 9874; b) S. Karlsson, H. Högberg, Tetrahedron: Asymmetry 2002, 13, 923; other reactions see: a) A. E. Taggi, A. M. Hafez, H. Wack, B. Young, W. J. Drury III, T. Lectka, J. Am. Chem. Soc. 2000, 121, 7831; b) B. R. Sculimbrene, A. J. Morgan, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 11653; c) M. Harmata, S. K. Ghosh, X. Hong, S. Wacharasindhu, P. Kirchhoefer, J. Am. Chem. Soc. 2003, 125, 2058; d) N. Bremeyer, S. C. Smith, S. V, Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735; Angew. Chem. Int. Ed. 2004, 43, 2681.
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    • c) T. Akiyama, J. Itoh, K. Yokota, K. Fuchibe, Angew. Chem. 2004, 116, 1592; Angew. Chem. Int. Ed. 2004, 43, 1566;
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    • b) Yamamoto, Saito and co-workers have also reported two excellent examples of organocatalytic asymmetric α-hydroxymethylation of ketones see: H. Torii, M. Nakadai, K. Ishihara, S. Saito, H. Yamamoto, Angew. Chem. 2004, 116, 2017; Angew. Chem. Int. Ed. 2004, 43, 1983.
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    • Torii, H.1    Nakadai, M.2    Ishihara, K.3    Saito, S.4    Yamamoto, H.5
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    • b) Yamamoto, Saito and co-workers have also reported two excellent examples of organocatalytic asymmetric α-hydroxymethylation of ketones see: H. Torii, M. Nakadai, K. Ishihara, S. Saito, H. Yamamoto, Angew. Chem. 2004, 116, 2017; Angew. Chem. Int. Ed. 2004, 43, 1983.
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    • note
    • The compounds are sensitive and racemize upon column chromatography with silica gel as the stationary phase. The Mannich base products should be stored at -35°C.
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    • and references therein
    • S. Bahmanyar, K. N. Houk, Org. Lett. 2003, 5, 1249 and references therein.
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    • Bahmanyar, S.1    Houk, K.N.2


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