메뉴 건너뛰기




Volumn 30, Issue 50, 1989, Pages 7075-7078

Enantioselective routes to 2,5-disubstituted- and 4-substituted-2-cyclohexenones

Author keywords

[No Author keywords available]

Indexed keywords

2 CYCLOHEXENONE DERIVATIVE;

EID: 0024810948     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)93427-6     Document Type: Article
Times cited : (16)

References (15)
  • 1
    • 84918612202 scopus 로고    scopus 로고
    • The Total Synthesis of Natural Products, ed by J.A. ApSimon, John Wiley & Sons, New York, Vol. 2; “Natural Products Chemistry,” ed by K. Nakanishi, T. Goto, S. Itoh, S. Natori, and S. Nozoe, Kodansha Ltd, Tokyo, Vol. 1.
  • 3
    • 84918646088 scopus 로고
    • Homologues ofp-Menthane Derivatives in Roman Camomile
    • Some papers have reported racemic and enantiomeric preparation of 2,5-disubstituted and 4-substituted cyclohexenones
    • (1981) Helvetica Chimica Acta , vol.64 , pp. 1488
    • Thomas1    Schouwey2    Egger3
  • 11
    • 84918604857 scopus 로고    scopus 로고
    • S.G. Levine and B. Gopalakrishnan, Tetrahedron Lett., 1979, 699
  • 13
    • 84918615151 scopus 로고    scopus 로고
    • Attempted enolate anion formation from 3-methoxy-5-trimethylsilyl-2-cyclohexenone, which could obtained from 5 with sodium methoxide in methanol in 85% yield, under a similar reaction conditions resulted in a failure.
  • 15
    • 84918610185 scopus 로고    scopus 로고
    • 3).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.