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Volumn 29, Issue 6, 1988, Pages 669-672

Palladium-catalyzed asymmetric intramolecular allylation forming optically active vinylcyclopropane and vinyldihydrofurans

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EID: 0001659220     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)80179-3     Document Type: Article
Times cited : (71)

References (29)
  • 7
    • 0037538809 scopus 로고
    • Asymmetric allylic alkylation of 1,3-disubstituted 2-propenyl acetates catalyzed by a chiral ferrocenylphosphine-palladium complex.
    • (1987) Chemistry Letters , pp. 177
    • Hayashi1    Yamamoto2    Ito3
  • 22
    • 84918176212 scopus 로고    scopus 로고
    • Syn stereochemistry has been reported in the palladium-catalyzed cyclization of an optically active functionalized allylic benzoate (ref 5d).
  • 25
    • 0002536278 scopus 로고
    • Palladium(0)-catalyzed cycloaddition of activated vinylcyclopropanes with aryl isocyanates.
    • Palladium-catalyzed reactions involving oxidative addition of vinylcyclopropane and related compounds to palladium(0) have been reported, ref 5a,b and
    • (1987) Chemistry Letters , pp. 1157
    • Yamamoto1    Ishida2    Tsuji3
  • 26
    • 84918176211 scopus 로고    scopus 로고
    • Epimerization of 5 can take place by π-σ-π rearrangement of the allylpalladium complex.
  • 27
    • 84918176210 scopus 로고    scopus 로고
    • 2 and diallylation products has been reported (ref 5a).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.