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Volumn 23, Issue 7, 2012, Pages 1085-1089

A transition-metal-free cross-coupling reaction of allylic bromides with aryl- and vinylboronic acids

Author keywords

aryl and vinylboronic acids; C C bond formation; transition metal free

Indexed keywords

ARYLBORONIC ACID; BORONIC ACID DERIVATIVE; BROMINE DERIVATIVE; CARBON; INORGANIC COMPOUND; METAL; UNCLASSIFIED DRUG; VINYLBORONIC ACID;

EID: 84859832543     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1290656     Document Type: Review
Times cited : (24)

References (63)
  • 35
    • 84859867245 scopus 로고    scopus 로고
    • Rh- and Ni-catalyzed cross-coupling reactions of allylic acetates, allylic amines, and allylic alcohols with arylboronic acids also have been reported, but, in these reactions, the range of applicable substrates was very narrow.
    • Rh- and Ni-catalyzed cross-coupling reactions of allylic acetates, allylic amines, and allylic alcohols with arylboronic acids also have been reported, but, in these reactions, the range of applicable substrates was very narrow.
  • 46
    • 84859878879 scopus 로고    scopus 로고
    • We also tested the reactivity of other organoboronic acid derivatives. Potassium 4-methoxyphenyltrifluoroborate was able to react with 1a, but the yield was low (25%). Pinacol ester of 1a did not work as a substrate.
    • We also tested the reactivity of other organoboronic acid derivatives. Potassium 4-methoxyphenyltrifluoroborate was able to react with 1a, but the yield was low (25%). Pinacol ester of 1a did not work as a substrate.
  • 47
    • 84859867783 scopus 로고    scopus 로고
    • 2O gave 3aa in a moderate yield (60%).
    • 2O gave 3aa in a moderate yield (60%).
  • 48
    • 84859878878 scopus 로고    scopus 로고
    • In the general conditions, phenylboronic acid (1h) gave the cross-coupling product 3ha in a poor yield (7% yield), and the reaction of 4-acetylphenylboronic acid with 2a did not give the corresponding product.
    • In the general conditions, phenylboronic acid (1h) gave the cross-coupling product 3ha in a poor yield (7% yield), and the reaction of 4-acetylphenylboronic acid with 2a did not give the corresponding product.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.