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Volumn 46, Issue 6, 2005, Pages 937-939

A route to the fully substituted cyclopentane unit of viridenomycin using a tandem radical cyclisation-trapping strategy

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; ANTINEOPLASTIC AGENT; CYCLOPENTANE; SILICON; TIN DERIVATIVE; UNCLASSIFIED DRUG; VIRIDENOMYCIN;

EID: 12344285710     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.12.063     Document Type: Article
Times cited : (15)

References (27)
  • 6
    • 0000103329 scopus 로고
    • The scope of this tether approach in the synthesis of substituted cyclopentanes was first highlighted by Stork et al. in their studies of prostaglandin synthesis: G. Stork, and P.M. Sher J. Am. Chem. Soc. 105 1983 6765 6766
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 6765-6766
    • Stork, G.1    Sher, P.M.2
  • 16
    • 12344327810 scopus 로고
    • For the development of radical traps in synthesis see: G.E. Keck, and D.A. Burnett J. Org. Chem. 52 1987 2960 and references cited therein
    • (1987) J. Org. Chem. , vol.52 , pp. 2960
    • Keck, G.E.1    Burnett, D.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.