메뉴 건너뛰기




Volumn 14, Issue 10, 1996, Pages 15-X32

Stereoselective synthesis of γ-butyrolactones by intramolecular michael addition

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0030515516     PISSN: 0392839X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (49)
  • 1
    • 0024451049 scopus 로고
    • and references cited therein
    • For reviews concerning the synthesis of butenolides and saturated γ-lactones see: a) Y. Nagao, W. Dai, M. Ochiai, M. Shiro; J. Org. Chem. 54 5211 (1989). and references cited therein b) E.J. Corey, X.M. Cheng: in: The Logic of Chemical Synthesis: John Wiley Sons, Inc., New York, 1989
    • (1989) J. Org. Chem. , vol.54 , pp. 5211
    • Nagao, Y.1    Dai, W.2    Ochiai, M.3    Shiro, M.4
  • 2
    • 0024451049 scopus 로고
    • John Wiley Sons, Inc., New York
    • For reviews concerning the synthesis of butenolides and saturated γ-lactones see: a) Y. Nagao, W. Dai, M. Ochiai, M. Shiro; J. Org. Chem. 54 5211 (1989). and references cited therein b) E.J. Corey, X.M. Cheng: in: The Logic of Chemical Synthesis: John Wiley Sons, Inc., New York, 1989
    • (1989) The Logic of Chemical Synthesis
    • Corey, E.J.1    Cheng, X.M.2
  • 6
    • 0345905188 scopus 로고
    • Dictionary of organic compounds
    • Chapman and Hall, NY, Ed. C. Hansch; Pergamon Press, Oxford, UK
    • Dictionary of Organic Compounds. Chapman and Hall, NY, 1982 Comprehensive Medicinal Chemistry, Ed. C. Hansch; Pergamon Press, Oxford, UK, 1990
    • (1982) Comprehensive Medicinal Chemistry
  • 38
    • 0001780886 scopus 로고    scopus 로고
    • L.A. Paquette et al. Eds.; Wiley, N.Y.
    • T. Katsuki, V.S. Martín; Org. React. L.A. Paquette et al. Eds.; Wiley, N.Y., 1996, Vol.48, pp. 1-299
    • (1996) Org. React. , vol.48 , pp. 1-299
    • Katsuki, T.1    Martín, V.S.2
  • 43
    • 0001247160 scopus 로고
    • The synthesis of (1R,2S)-( + )-grandisol (J.H. Tumlinson, R.C. Gueldner, D.D. Hardee, A.C. Thompson, P.A. Hedin, J.P. Minyard; J. Org. Chem. 36 2616 (1971), a component of the boll weevil pheromone, has been performed using as the main step the described methodology: T. Martín, C.M. Rodríguez, V.S. Martín; Tetrahedron: Asymmetry 6 1151 (1995)
    • (1971) J. Org. Chem. , vol.36 , pp. 2616
    • Tumlinson, J.H.1    Gueldner, R.C.2    Hardee, D.D.3    Thompson, A.C.4    Hedin, P.A.5    Minyard, J.P.6
  • 44
    • 0029007420 scopus 로고
    • The synthesis of (1R,2S)-( + )-grandisol (J.H. Tumlinson, R.C. Gueldner, D.D. Hardee, A.C. Thompson, P.A. Hedin, J.P. Minyard; J. Org. Chem. 36 2616 (1971), a component of the boll weevil pheromone, has been performed using as the main step the described methodology: T. Martín, C.M. Rodríguez, V.S. Martín; Tetrahedron: Asymmetry 6 1151 (1995)
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 1151
    • Martín, T.1    Rodríguez, C.M.2    Martín, V.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.