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Volumn 40, Issue 12, 1984, Pages 2317-2327

Electrophilic lactonization as a tool in acyclic stereocontrol. Synthesis of serricornin

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Indexed keywords


EID: 0001631004     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(84)80015-0     Document Type: Article
Times cited : (115)

References (57)
  • 1
    • 84918093817 scopus 로고    scopus 로고
    • Reviews: P. A. Bartlett, Asymmetric Synthesis vol. 3., Chap 6. (Edited by J. D. Morrison), Academic Press, New York, in press
  • 18
    • 0010235022 scopus 로고
    • A novel method for the synthesis of 2-deoxydisaccharide by stereoselective cyclization of the acyclic precursor.
    • Inter alia
    • (1982) Chemistry Letters , pp. 683
    • Suzuki1    Mukaiyma2
  • 48
    • 84918093816 scopus 로고    scopus 로고
    • These attempts is included direct ketalization of 28 with ethylene glycol followed by inversion of the alcohol, and simultaneous opening of the hemiacetal and activation of the secondary OH with tosyl chloride in pyridine.
  • 49
    • 85077634689 scopus 로고
    • The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
    • (1981) Synthesis , pp. 1
    • Mitsunobu1
  • 55
    • 84918093815 scopus 로고    scopus 로고
    • F. Bermejo Ganzalez and P.A. Bartlett, Org. Syn. in press.
  • 56
    • 85066134647 scopus 로고
    • Recommended Work-up Procedure for Reductions Employing Tri-n-butyltin Hydride
    • (1979) Synthesis , pp. 471
    • Berge1    Roberts2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.