메뉴 건너뛰기




Volumn 44, Issue 1, 2004, Pages 108-110

Metal-free, organocatalytic asymmetric transfer hydrogenation of α,β-unsaturated aldehydes

Author keywords

Asymmetric catalysis; Chemoselectivity; Enantioselectivity; Hydrogenation; Organocatalysis

Indexed keywords

ALDEHYDE; ALKENE; DIHYDROPYRIDINE DERIVATIVE; NATURAL PRODUCT;

EID: 11244320360     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200462432     Document Type: Article
Times cited : (168)

References (28)
  • 1
    • 0001552544 scopus 로고    scopus 로고
    • a) R. Noyori, Angew. Chem. 2002, 114, 2108-2123; Angew. Chem. Int. Ed. 2002, 41, 2008-2022;
    • (2002) Angew. Chem. , vol.114 , pp. 2108-2123
    • Noyori, R.1
  • 2
    • 0037124885 scopus 로고    scopus 로고
    • a) R. Noyori, Angew. Chem. 2002, 114, 2108-2123; Angew. Chem. Int. Ed. 2002, 41, 2008-2022;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2008-2022
  • 3
    • 0000370001 scopus 로고    scopus 로고
    • b) W. S. Knowles, Angew. Chem. 2002, 114, 2096-2107; Angew. Chem. Int. Ed. 2002, 41, 1998-2007.
    • (2002) Angew. Chem. , vol.114 , pp. 2096-2107
    • Knowles, W.S.1
  • 4
    • 0037124758 scopus 로고    scopus 로고
    • b) W. S. Knowles, Angew. Chem. 2002, 114, 2096-2107; Angew. Chem. Int. Ed. 2002, 41, 1998-2007.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1998-2007
  • 6
    • 0037167050 scopus 로고    scopus 로고
    • For mechanistic studies on the base-catalyzed and transition-metal-free hydrogenation of ketones, see: a) A. Berkessel, T. J. S. Schubert, T. N. Müller, J. Am. Chem. Soc. 2002, 124, 8693-8698; Also see: b) J. H. Teles, S. Brode, A. Berkessel, J. Am. Chem. Soc. 1998, 120, 1345-1346; c) E. J. Lyon, S. Shima, G. Buurman, S. Chowdhuri, A. Batschauer, K. Steinbach, R. K. Thauer, Eur. J. Biochem. 2004, 271, 195-204.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 8693-8698
    • Berkessel, A.1    Schubert, T.J.S.2    Müller, T.N.3
  • 7
    • 0001015102 scopus 로고    scopus 로고
    • For mechanistic studies on the base-catalyzed and transition-metal-free hydrogenation of ketones, see: a) A. Berkessel, T. J. S. Schubert, T. N. Müller, J. Am. Chem. Soc. 2002, 124, 8693-8698; Also see: b) J. H. Teles, S. Brode, A. Berkessel, J. Am. Chem. Soc. 1998, 120, 1345-1346; c) E. J. Lyon, S. Shima, G. Buurman, S. Chowdhuri, A. Batschauer, K. Steinbach, R. K. Thauer, Eur. J. Biochem. 2004, 271, 195-204.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 1345-1346
    • Teles, J.H.1    Brode, S.2    Berkessel, A.3
  • 8
    • 1642580510 scopus 로고    scopus 로고
    • For mechanistic studies on the base-catalyzed and transition-metal-free hydrogenation of ketones, see: a) A. Berkessel, T. J. S. Schubert, T. N. Müller, J. Am. Chem. Soc. 2002, 124, 8693-8698; Also see: b) J. H. Teles, S. Brode, A. Berkessel, J. Am. Chem. Soc. 1998, 120, 1345-1346; c) E. J. Lyon, S. Shima, G. Buurman, S. Chowdhuri, A. Batschauer, K. Steinbach, R. K. Thauer, Eur. J. Biochem. 2004, 271, 195-204.
    • (2004) Eur. J. Biochem. , vol.271 , pp. 195-204
    • Lyon, E.J.1    Shima, S.2    Buurman, G.3    Chowdhuri, S.4    Batschauer, A.5    Steinbach, K.6    Thauer, R.K.7
  • 10
    • 0001644556 scopus 로고    scopus 로고
    • P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840-3864; Angew. Chem. Int. Ed. 2001, 40, 3726-3748.
    • (2001) Angew. Chem. , vol.113 , pp. 3840-3864
    • Dalko, P.I.1    Moisan, L.2
  • 11
    • 0035886887 scopus 로고    scopus 로고
    • P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840-3864; Angew. Chem. Int. Ed. 2001, 40, 3726-3748.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 3726-3748
  • 12
  • 13
    • 10944220196 scopus 로고    scopus 로고
    • DOI: 10.1002/anie.200461816
    • J. W. Yang, M. T. Hechavarria Fonseca, B. List, Angew. Chem. 2004, 116, DOI: 10.1002/ange.200461816; Angew. Chem. Int. Ed. 2004, 43, DOI: 10.1002/anie.200461816.
    • (2004) Angew. Chem. Int. Ed. , vol.43
  • 14
    • 0006098805 scopus 로고
    • For examples of transition-metal-catalyzed asymmetric conjugate reductions of amides, esters, ketones, and nitroalkenes, see: a) U. Leutenegger, A. Madin, A. Pfaltz, Angew. Chem. 1989, 101, 61-62; Angew. Chem. Int. Ed. Engl. 1989, 28, 60; b) D. H. Appella, Y. Moritani, R. Shintani, E. M. Ferreira, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9473-9474; c) B. H. Lipshutz, J. M. Servesko, Angew. Chem. 2003, 115, 4937-4940; Angew. Chem. Int. Ed. 2003, 42, 4789-4792; d) C. Czekelius, E. M. Carreira, Angew. Chem. 2003, 115, 4941-4943; Angew. Chem. Int. Ed. 2003, 42, 4793-4795.
    • (1989) Angew. Chem. , vol.101 , pp. 61-62
    • Leutenegger, U.1    Madin, A.2    Pfaltz, A.3
  • 15
    • 0042511206 scopus 로고
    • For examples of transition-metal-catalyzed asymmetric conjugate reductions of amides, esters, ketones, and nitroalkenes, see: a) U. Leutenegger, A. Madin, A. Pfaltz, Angew. Chem. 1989, 101, 61-62; Angew. Chem. Int. Ed. Engl. 1989, 28, 60; b) D. H. Appella, Y. Moritani, R. Shintani, E. M. Ferreira, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9473-9474; c) B. H. Lipshutz, J. M. Servesko, Angew. Chem. 2003, 115, 4937-4940; Angew. Chem. Int. Ed. 2003, 42, 4789-4792; d) C. Czekelius, E. M. Carreira, Angew. Chem. 2003, 115, 4941-4943; Angew. Chem. Int. Ed. 2003, 42, 4793-4795.
    • (1989) Angew. Chem. Int. Ed. Engl. , vol.28 , pp. 60
  • 16
    • 0033552259 scopus 로고    scopus 로고
    • For examples of transition-metal-catalyzed asymmetric conjugate reductions of amides, esters, ketones, and nitroalkenes, see: a) U. Leutenegger, A. Madin, A. Pfaltz, Angew. Chem. 1989, 101, 61-62; Angew. Chem. Int. Ed. Engl. 1989, 28, 60; b) D. H. Appella, Y. Moritani, R. Shintani, E. M. Ferreira, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9473-9474; c) B. H. Lipshutz, J. M. Servesko, Angew. Chem. 2003, 115, 4937-4940; Angew. Chem. Int. Ed. 2003, 42, 4789-4792; d) C. Czekelius, E. M. Carreira, Angew. Chem. 2003, 115, 4941-4943; Angew. Chem. Int. Ed. 2003, 42, 4793-4795.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 9473-9474
    • Appella, D.H.1    Moritani, Y.2    Shintani, R.3    Ferreira, E.M.4    Buchwald, S.L.5
  • 17
    • 10944255551 scopus 로고    scopus 로고
    • For examples of transition-metal-catalyzed asymmetric conjugate reductions of amides, esters, ketones, and nitroalkenes, see: a) U. Leutenegger, A. Madin, A. Pfaltz, Angew. Chem. 1989, 101, 61-62; Angew. Chem. Int. Ed. Engl. 1989, 28, 60; b) D. H. Appella, Y. Moritani, R. Shintani, E. M. Ferreira, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9473-9474; c) B. H. Lipshutz, J. M. Servesko, Angew. Chem. 2003, 115, 4937-4940; Angew. Chem. Int. Ed. 2003, 42, 4789-4792; d) C. Czekelius, E. M. Carreira, Angew. Chem. 2003, 115, 4941-4943; Angew. Chem. Int. Ed. 2003, 42, 4793-4795.
    • (2003) Angew. Chem. , vol.115 , pp. 4937-4940
    • Lipshutz, B.H.1    Servesko, J.M.2
  • 18
    • 0142183577 scopus 로고    scopus 로고
    • For examples of transition-metal-catalyzed asymmetric conjugate reductions of amides, esters, ketones, and nitroalkenes, see: a) U. Leutenegger, A. Madin, A. Pfaltz, Angew. Chem. 1989, 101, 61-62; Angew. Chem. Int. Ed. Engl. 1989, 28, 60; b) D. H. Appella, Y. Moritani, R. Shintani, E. M. Ferreira, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9473-9474; c) B. H. Lipshutz, J. M. Servesko, Angew. Chem. 2003, 115, 4937-4940; Angew. Chem. Int. Ed. 2003, 42, 4789-4792; d) C. Czekelius, E. M. Carreira, Angew. Chem. 2003, 115, 4941-4943; Angew. Chem. Int. Ed. 2003, 42, 4793-4795.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 4789-4792
  • 19
    • 10044257201 scopus 로고    scopus 로고
    • For examples of transition-metal-catalyzed asymmetric conjugate reductions of amides, esters, ketones, and nitroalkenes, see: a) U. Leutenegger, A. Madin, A. Pfaltz, Angew. Chem. 1989, 101, 61-62; Angew. Chem. Int. Ed. Engl. 1989, 28, 60; b) D. H. Appella, Y. Moritani, R. Shintani, E. M. Ferreira, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9473-9474; c) B. H. Lipshutz, J. M. Servesko, Angew. Chem. 2003, 115, 4937-4940; Angew. Chem. Int. Ed. 2003, 42, 4789-4792; d) C. Czekelius, E. M. Carreira, Angew. Chem. 2003, 115, 4941-4943; Angew. Chem. Int. Ed. 2003, 42, 4793-4795.
    • (2003) Angew. Chem. , vol.115 , pp. 4941-4943
    • Czekelius, C.1    Carreira, E.M.2
  • 20
    • 0142183590 scopus 로고    scopus 로고
    • For examples of transition-metal-catalyzed asymmetric conjugate reductions of amides, esters, ketones, and nitroalkenes, see: a) U. Leutenegger, A. Madin, A. Pfaltz, Angew. Chem. 1989, 101, 61-62; Angew. Chem. Int. Ed. Engl. 1989, 28, 60; b) D. H. Appella, Y. Moritani, R. Shintani, E. M. Ferreira, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9473-9474; c) B. H. Lipshutz, J. M. Servesko, Angew. Chem. 2003, 115, 4937-4940; Angew. Chem. Int. Ed. 2003, 42, 4789-4792; d) C. Czekelius, E. M. Carreira, Angew. Chem. 2003, 115, 4941-4943; Angew. Chem. Int. Ed. 2003, 42, 4793-4795.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 4793-4795
  • 22
    • 0034750244 scopus 로고    scopus 로고
    • b) B. List, Synlett 2001, 1675-1686;
    • (2001) Synlett , pp. 1675-1686
    • List, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.