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银催化的有机锌试剂对三级溴代烷烃的苄基化和烯丙基化反应。

Silver-catalyzed benzylation and allylation of tertiary alkyl bromides with organozinc reagents.

机构信息

Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto-daigaku Katsura, Nishikyo, Kyoto 615-8510, Japan.

出版信息

Chem Asian J. 2010 Jun 1;5(6):1487-93. doi: 10.1002/asia.201000068.

DOI:10.1002/asia.201000068
PMID:20446338
Abstract

Silver salts catalyze the benzylation and allylation of tertiary alkyl bromides with organozinc reagents. The reactions create quaternary carbon centers efficiently. Treatment of gem-dibromoalkanes with benzylic or allylic zinc reagents under silver catalysis leads to dibenzylation or diallylation. The functional-group compatibility of the present reactions is wider than that of the previous reactions with Grignard reagents.

摘要

银盐催化有机锌试剂对叔烷基溴化物的苄基化和烯丙基化反应。这些反应有效地生成了季碳原子中心。在银催化下,用苄基或烯丙基锌试剂处理偕二溴烷烃,可得到二苄基或二烯丙基产物。与之前用格氏试剂进行的反应相比,本反应的官能团兼容性更广泛。

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