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Volumn 354, Issue 5, 2012, Pages 828-834

Cyclopropanation of strained alkenes by palladium-catalyzed reaction of 3-trimethylsilyl- or 3-pinacolatoboryl-1-arylallyl acetates

Author keywords

allylpalladium species; allylsilanes; cyclopropanation; palladacyclobutenes; palladium carbenoids

Indexed keywords


EID: 84858761448     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201100806     Document Type: Article
Times cited : (23)

References (61)
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  • 61
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    • An alternative mechanism involves insertion of 2a to a π-allylpalladium intermediate that would be produced by palladium complexing with cinnamyl acetate generated from protodesilylation of 1a. However, this process preferentially produces a [2+2] cycloadduct rather than a cyclopropanation product, thus making this possibility rather unlikely. For details, see
    • An alternative mechanism involves insertion of 2a to a π-allylpalladium intermediate that would be produced by palladium complexing with cinnamyl acetate generated from protodesilylation of 1a. However, this process preferentially produces a [2+2] cycloadduct rather than a cyclopropanation product, thus making this possibility rather unlikely. For details, see:, N. Tsukada, T. Sato, Y. Inoue, Tetrahedron Lett. 2000, 41, 4181-4184.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 4181-4184
    • Tsukada, N.1    Sato, T.2    Inoue, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.