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Volumn 42, Issue 13-14, 1997, Pages 1967-1970

Intramolecular anodic olefin coupling reactions: The use of an allylic alkoxy group for controlling relative stereochemistry

Author keywords

Intramolecular anodic olefin coupling; Stereochemistry

Indexed keywords

ANODIC OXIDATION; CONFORMATIONS; ELECTROCHEMISTRY; REACTION KINETICS; SUBSTRATES; SYNTHESIS (CHEMICAL);

EID: 0030652690     PISSN: 00134686     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0013-4686(97)85468-0     Document Type: Article
Times cited : (9)

References (18)
  • 7
    • 0027396756 scopus 로고
    • For a prior total synthesis of crinipellin B see (a) E. Piers and J. Renaud, J. Org. Chem. 25, 11-13 (1993). For prior synthetic efforts see
    • (1993) J. Org. Chem. , vol.25 , pp. 11-13
    • Piers, E.1    Renaud, J.2
  • 13
    • 0039352796 scopus 로고    scopus 로고
    • note
    • When the substrate containing the alcohol was electrolysed, no product resulting from carbon-carbon bond formation was obtained. Only tetrahydrofuranbased products were isolated.
  • 15
    • 0039945128 scopus 로고    scopus 로고
    • note
    • Alcohol 6 was synthesized from 1,4-butanediol by protecting one of the alcohols using TBDMSCI, oxidizing the second alcohol to an aldehyde using Swern conditions, forming the enol ether with the use of a Wittig reaction, and then deprotecting the silyl ether using TBAF.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.