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Volumn 14, Issue 1, 2008, Pages 325-332

Diastereoselective synthesis of three-, five-, six-, and seven-membered rings from fischer carbene complexes and 4-unsubstituted 1-amino-1,3-dienes

Author keywords

Aminodienes; Carbenes; Cyclization; Diastereoselectivity; Organic synthesis

Indexed keywords

CARBON; COMPLEXATION; CYCLIZATION; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

EID: 38049176503     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200701109     Document Type: Article
Times cited : (11)

References (64)
  • 2
    • 38049147274 scopus 로고    scopus 로고
    • R. D. Little in Comprehensive Organic Synthesis, 5 (Eds.: M. Trost, I. Fleming), Pergamon Press, Oxford, 1991, Chapter 3.1B, pp. 239-270;
    • b) R. D. Little in Comprehensive Organic Synthesis, Vol. 5 (Eds.: M. Trost, I. Fleming), Pergamon Press, Oxford, 1991, Chapter 3.1B, pp. 239-270;
  • 3
    • 0000384028 scopus 로고    scopus 로고
    • Eds, M. Trost, I. Fleming, Chapter 3.2, pp
    • c) D. M. T. Chan in Comprehensive Organic Synthesis, Vol. 5 (Eds.: M. Trost, I. Fleming), Chapter 3.2, pp. 271-314;
    • Comprehensive Organic Synthesis , vol.5 , pp. 271-314
    • Chan, D.M.T.1
  • 4
    • 0000646877 scopus 로고    scopus 로고
    • Eds, M. Trost, I. Fleming, Chapter 6.3, pp
    • d) S. E. Denmark in Comprehensive Organic Synthesis, Vol. 5 (Eds.: M. Trost, I. Fleming), Chapter 6.3, pp. 751-784;
    • Comprehensive Organic Synthesis , vol.5 , pp. 751-784
    • Denmark, S.E.1
  • 7
    • 38049139916 scopus 로고    scopus 로고
    • T. Hudlicky, F. Rulin, T. C. Lovelace, J. W. Reed in Studies in Natural Products Chemistry (Ed.: T., Attaur-Rahman), Elsevier Science, Essex, U.K., 1989.
    • b) T. Hudlicky, F. Rulin, T. C. Lovelace, J. W. Reed in Studies in Natural Products Chemistry (Ed.: T., Attaur-Rahman), Elsevier Science, Essex, U.K., 1989.
  • 9
    • 0038524273 scopus 로고    scopus 로고
    • For recent reviews see: a
    • For recent reviews see: a) K. H. Dötz, P. Tomuschat, Chem. Soc. Rev. 1999, 28, 187-198;
    • (1999) Chem. Soc. Rev , vol.28 , pp. 187-198
    • Dötz, K.H.1    Tomuschat, P.2
  • 12
    • 34250831135 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 3964-4002;
    • (2000) Chem. Int. Ed , vol.39 , pp. 3964-4002
    • Angew1
  • 13
    • 0034301372 scopus 로고    scopus 로고
    • d) M. A. Sierra, Chem. Rev. 2000, 100, 3591-3637;
    • (2000) Chem. Rev , vol.100 , pp. 3591-3637
    • Sierra, M.A.1
  • 23
    • 0000134377 scopus 로고
    • Eds, E. W. Abel, F. G. A. Stone, G. Wilkinson, Pergamon, Oxford
    • a) W. D. Wulff in Comprehensive Organometallic Chemistry II, Vol. 12 (Eds.: E. W. Abel, F. G. A. Stone, G. Wilkinson), Pergamon, Oxford, 1995, pp. 469-547;
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 469-547
    • Wulff, W.D.1
  • 40
    • 0037420313 scopus 로고    scopus 로고
    • The substitution pattern has been shown to play an important role on the reactivity of alkenyl carbene complexes and methyl ketone lithium enolates. See for example: a J. Barluenga, J. Alonso, F. J. Fañanás, J. Am. Chem. Soc. 2003, 125, 2610-2616;
    • The substitution pattern has been shown to play an important role on the reactivity of alkenyl carbene complexes and methyl ketone lithium enolates. See for example: a) J. Barluenga, J. Alonso, F. J. Fañanás, J. Am. Chem. Soc. 2003, 125, 2610-2616;
  • 47
    • 0001309333 scopus 로고
    • For 1,2-metal migrations see: a
    • For 1,2-metal migrations see: a) H. Fischer, T. Meisner, J. Hofmann, Chem. Ber. 1990, 123, 1799-1804;
    • (1990) Chem. Ber , vol.123 , pp. 1799-1804
    • Fischer, H.1    Meisner, T.2    Hofmann, J.3
  • 55
    • 0033583546 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 1091-1093.
    • (1999) Chem. Int. Ed , vol.38 , pp. 1091-1093
    • Angew1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.