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Volumn 53, Issue 32, 1997, Pages 11061-11068

Synthesis of pyranose glycals via tungsten and molybdenum pentacarbonyl-induced alkynol cyclizations

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC ANTIBIOTIC; PLURAMYCIN; VANCOMYCIN;

EID: 0030852174     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00366-9     Document Type: Article
Times cited : (47)

References (29)
  • 18
    • 0026525188 scopus 로고
    • For the preparation of a similar glycal from the antibiotic natural product vancomycin, see: Dushin, R. G.; Danishefsky, S. J. J. Am. Chem. Soc. 1992, 114, 3471.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 3471
    • Dushin, R.G.1    Danishefsky, S.J.2
  • 22
    • 0343095785 scopus 로고    scopus 로고
    • note
    • A similar sequence of reactions was used to convert Z-12 into alkynol i (the C4-diastereomer of 17). However, substrate i could not be cleanly converted into either the corresponding carbene ii or the pyranose glycal iii, and this route was not further pursued. (formula presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.