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Volumn 62, Issue 3, 1997, Pages 454-455

Enantioselective synthesis of the elaiophylin aglycon

Author keywords

[No Author keywords available]

Indexed keywords

ELAIOLIDE; ELAIOPHYLIN; MACROCYCLIC COMPOUND; UNCLASSIFIED DRUG;

EID: 0031038054     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9621884     Document Type: Article
Times cited : (65)

References (33)
  • 4
    • 8044259287 scopus 로고    scopus 로고
    • Salbomycin: Hoechst Patent DE 3248-280-A, 1972
    • Salbomycin: Hoechst Patent DE 3248-280-A, 1972.
  • 20
    • 0026327529 scopus 로고
    • A notable exception is the approach of Ziegler and co-workers, which involves the design of a fully elaborated monomeric fragment suitable for dimerization: Ziegler, F. E.; Tung, J. S. J. Org. Chem. 1991, 56, 6530.
    • (1991) J. Org. Chem. , vol.56 , pp. 6530
    • Ziegler, F.E.1    Tung, J.S.2
  • 22
    • 8044223718 scopus 로고
    • Ph.D. Dissertation, Harvard University
    • (b) Calter, M. A. Ph.D. Dissertation, Harvard University, 1993.
    • (1993)
    • Calter, M.A.1
  • 24
    • 8044221217 scopus 로고    scopus 로고
    • note
    • 2NEt provided a 3:1 mixture of isomers, favoring the desired anti-Felkin, syn aldol adduct (see ref 12c).
  • 26
    • 15844376790 scopus 로고    scopus 로고
    • For a recent study on the effects of a and β aldehyde substituents on the diasterecselectivity of allylstannane additions see: Evans, D. A.; Dart, M. J.; Duffy, J. L.; Yang, M. G. J. Am. Chem. Soc. 1996, 118, 4322.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 4322
    • Evans, D.A.1    Dart, M.J.2    Duffy, J.L.3    Yang, M.G.4
  • 30
    • 8044224963 scopus 로고    scopus 로고
    • 1H NMR analysis of the unpurified reaction mixture
    • 1H NMR analysis of the unpurified reaction mixture.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.