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Volumn 45, Issue 34, 2004, Pages 6457-6460

Alkoxy group facilitated ring closing metathesis (RCM) of acyclic 1,6-dienes. Convenient synthesis of non-racemic highly substituted cyclopentenols

Author keywords

Asymmetric synthesis; Cyclopentenes; Metathesis; Nucleosides

Indexed keywords

ABACAVIR; ALCOHOL DERIVATIVE; ALKADIENE; ALKENE DERIVATIVE; ANTIVIRUS AGENT; BIS(HYDROXYMETHYL)CYCLOPENTENYLADENINE; CARBOVIR; CHLORINE; METHYL GROUP; RUTHENIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 4143060245     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.06.127     Document Type: Article
Times cited : (30)

References (36)
  • 1
    • 0032490986 scopus 로고    scopus 로고
    • For recent reviews on the synthesis of carbocyclic nucleosides, see: M.T. Crimmins Tetrahedron 54 1998 9229 9272
    • (1998) Tetrahedron , vol.54 , pp. 9229-9272
    • Crimmins, M.T.1
  • 33
    • 4143138145 scopus 로고    scopus 로고
    • note
    • 2), 78.5 (OCH), 134.2 (CH), 136.1 (CH)
  • 35
    • 4143108509 scopus 로고    scopus 로고
    • note
    • The preparation of the dienol 1c and details of the stereochemical assignment of the dienol 21 will be described in a full account of this work


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.