메뉴 건너뛰기




Volumn 22, Issue 33, 1981, Pages 3119-3122

A new, highly efficient method for the conversion of alcohols to thiolesters and thiols

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000595912     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)81842-6     Document Type: Article
Times cited : (237)

References (18)
  • 1
    • 0010704954 scopus 로고
    • NEW SYNTHETIC REACTIONS BASED ON 1-METHYL-2-FLUOROPYRIDINIUM SALTS. STEREOSPECIFIC PREPARATION OF THIOALCOHOLS FROM ALCOHOLS
    • (1977) Chemistry Letters , pp. 437
    • Hojo1    Yoshino2    Mukaiyama3
  • 10
    • 85077634689 scopus 로고
    • The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
    • and references within
    • (1981) Synthesis , pp. 1
    • Mitsunobu1
  • 12
    • 84918366308 scopus 로고    scopus 로고
    • Preformation of the triphenylphosphine-diisopropyl azodicarboxylate adduct is essential for the success of this reaction. The standard sequence of reagent additions results in preliminary deactivation of the azodicarboxylate reagent by reaction with the thiolacid.
  • 15
    • 84918366307 scopus 로고
    • Merck and Co., Inc, Rahway, N.J
    • (1976) Merck Index , vol.9 , pp. 9052


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.