메뉴 건너뛰기




Volumn 46, Issue 40, 2007, Pages 7664-7666

An alkyne strategy for the asymmetric synthesis of natural products: Application to (+)-spirolaxine methyl ether

Author keywords

Alkynes; Asymmetric synthesis; Natural products; Spiro compounds; Total synthesis

Indexed keywords

ALKYNE STRATEGIES; ALKYNYLATIONS; ASYMMETRIC SYNTHESIS; BUILDING BLOCKS;

EID: 35048877537     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200702637     Document Type: Article
Times cited : (87)

References (46)
  • 1
    • 0003405157 scopus 로고    scopus 로고
    • In regard to the ketone: No other functional group can rival its versatility and utility. See:, Thieme, Stuttgart
    • In regard to the ketone: "No other functional group can rival its versatility and utility." See: P. J. Kocienski, Protecting Groups, Thieme, Stuttgart, 2005.
    • (2005) Protecting Groups
    • Kocienski, P.J.1
  • 4
    • 0003799267 scopus 로고
    • Eds, P. J. Stang, F. Diederich, VCH, Weinheim
    • Modern Acetylene Chemistry (Eds.: P. J. Stang, F. Diederich), VCH, Weinheim, 1995.
    • (1995) Modern Acetylene Chemistry
  • 5
    • 0003543593 scopus 로고    scopus 로고
    • Alkynes can readily be converted into ketones; see:, VCH, New York, NY
    • Alkynes can readily be converted into ketones; see: R. C. Larock, Comprehensive Organic Transformations, VCH, New York, NY, 1999.
    • (1999) Comprehensive Organic Transformations
    • Larock, R.C.1
  • 6
    • 0001800335 scopus 로고
    • For selected reviews, see: a
    • For selected reviews, see: a) K. P. C. Vollhardt, Acc. Chem. Res. 1977, 10, 1;
    • (1977) Acc. Chem. Res , vol.10 , pp. 1
    • Vollhardt, K.P.C.1
  • 9
    • 0742298948 scopus 로고    scopus 로고
    • For selected reviews, see: a
    • For selected reviews, see: a) B. M. Trost, M. J. Krische, Synlett 1998, 1;
    • (1998) Synlett , pp. 1
    • Trost, B.M.1    Krische, M.J.2
  • 14
    • 35048880761 scopus 로고    scopus 로고
    • M. A. Gaudliana, L. H. Huang, T. Kaneko, P. C. Watts, PCT Int. Appl. W0 9605204, 1996;
    • b) M. A. Gaudliana, L. H. Huang, T. Kaneko, P. C. Watts, PCT Int. Appl. W0 9605204, 1996;
  • 15
    • 35048852699 scopus 로고    scopus 로고
    • T. Adachi, I. Takagi, K. Kondo, A. Kawashima, A. Kobayashi, I. Taneoka, S. Morimoto, B. M. Hi, Z. Chen, PCT Int. Appl. W0 9610020, 1996.
    • c) T. Adachi, I. Takagi, K. Kondo, A. Kawashima, A. Kobayashi, I. Taneoka, S. Morimoto, B. M. Hi, Z. Chen, PCT Int. Appl. W0 9610020, 1996.
  • 27
    • 0242635970 scopus 로고    scopus 로고
    • f) L. Pu, Tetrahedron 2003, 59, 9873;
    • (2003) Tetrahedron , vol.59 , pp. 9873
    • Pu, L.1
  • 32
  • 34
    • 0003592858 scopus 로고
    • For a review, see:, 2nd ed, W. A. Benjamin, Menlo Park, CA
    • For a review, see: H. O. House, Modern Synthetic Reactions, 2nd ed., W. A. Benjamin, Menlo Park, CA, 1972.
    • (1972) Modern Synthetic Reactions
    • House, H.O.1
  • 35
    • 17744395347 scopus 로고    scopus 로고
    • Recent review: B. M. Trost, Z. T. Ball, Synthesis 2005, 853.
    • Recent review: B. M. Trost, Z. T. Ball, Synthesis 2005, 853.
  • 45


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.