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Volumn , Issue 11, 1997, Pages 1149-1150

Regioselective ring-opening of cyclopropyl ketones with organometallic reagents

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[No Author keywords available]

Indexed keywords


EID: 0031314569     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1997.1149     Document Type: Article
Times cited : (23)

References (26)
  • 21
    • 84971055615 scopus 로고
    • The nickel catalyzed conjugate addition of trimethylaluminum to α,β-unsaturated ketones has been reported: a) L. Bagnell, E. A. Jeffery, A. Meisters, and T. Mole, Aust. J. Chem., 28, 801 (1975).
    • (1975) Aust. J. Chem. , vol.28 , pp. 801
    • Bagnell, L.1    Jeffery, E.A.2    Meisters, A.3    Mole, T.4
  • 23
    • 0039642316 scopus 로고    scopus 로고
    • note
    • 3-Phenyl-2-butene-1-one was isolated as a by-product in less than 10% yield.
  • 25
    • 33947485009 scopus 로고
    • Compounds 9 and 10 were prepared from the reaction of the corresponding trans-enones with dimethyloxosulfonium methylide or (N,N-dimethylamino)methyloxosulphonium methylide: a) E. J. Corey and M. Chaykovsky, J. Am. Chem. Soc., 87, 1353 (1965).
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 1353
    • Corey, E.J.1    Chaykovsky, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.