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Volumn 69, Issue 4, 1996, Pages 1029-1031

A Convenient Route to β,γ-Unsaturated Esters without Formation of the α,β-Isomers. Palladium-Catalyzed Alkoxycarbonylation of Allylic Halides under Alcohol-Potassium Carbonate Tow-Phase Conditions

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Indexed keywords


EID: 0000329761     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.69.1029     Document Type: Article
Times cited : (24)

References (17)
  • 16
    • 33847087671 scopus 로고
    • A. Cowell and J. K. Stille, J. Am. Chem. Soc., 102, 4193 (1980). They used a phosphine-modified palladium carbonyl as the catalyst. It is thought that this low turnover number results from the use of a phosphine-containing catalyst.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 4193
    • Cowell, A.1    Stille, J.K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.