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Volumn 52, Issue 13, 1996, Pages 4757-4768

Studies on the synthesis of tunicamycin. The preparation of 7-deoxy-2-deamino-6-hydroxy tunicamine and related products

Author keywords

[No Author keywords available]

Indexed keywords

TUNICAMYCIN;

EID: 0343881993     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00146-9     Document Type: Article
Times cited : (30)

References (44)
  • 23
    • 0004164846 scopus 로고
    • The Royal Society of Chemistry, London
    • M.L. Sinnot, Enzyme Mechanisms, The Royal Society of Chemistry, London, 1987, p 259.
    • (1987) Enzyme Mechanisms , pp. 259
    • Sinnot, M.L.1
  • 41
    • 85030195516 scopus 로고    scopus 로고
    • note
    • 2); 18.6 (SMe). Alkaline hydrolysis of this product yielded the starting alcohol 12.
  • 44
    • 33845561484 scopus 로고
    • Equation presented
    • The moderate yield of the azido derivative 21 from the tosylated product 20 was a result of the formation of the corresponding elimination products 23 and 24. The structure of the alkene 24 was demonstrated by comparison with data reported by J. A. Secrist III and S. R. Wu (J. Org. Chem., 1979, 44, 1434). Equation presented
    • (1979) J. Org. Chem. , vol.44 , pp. 1434
    • Secrist J.A. III1    Wu, S.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.