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一种用于芳基格氏试剂与伯烷基和仲烷基溴进行化学选择性钴催化交叉偶联的新型高效催化体系。

A new efficient catalytic system for the chemoselective cobalt-catalyzed cross-coupling of aryl Grignard reagents with primary and secondary alkyl bromides.

作者信息

Cahiez Gérard, Chaboche Christophe, Duplais Christophe, Moyeux Alban

机构信息

Department of Chemistry, CNRS-Universite de Paris13, 74 Rue Marcel Cachin, F-93017 Bobigny, France.

出版信息

Org Lett. 2009 Jan 15;11(2):277-80. doi: 10.1021/ol802362e.

Abstract

The cobalt-catalyzed alkylation of aromatic Grignard reagents is performed in good yields by using a new simple and efficient catalytic system: CoCl(2)/TMEDA (1:1). Primary and secondary cyclic or acyclic alkyl bromides were used successfully. The reaction is highly chemoselective since ester, amide, and keto groups are tolerated. The procedure is inexpensive and very easy to carry out on a larger scale.

摘要

通过使用一种新型简单高效的催化体系

CoCl(2)/TMEDA(1:1),可实现钴催化的芳香格氏试剂的烷基化反应,且产率良好。伯烷基、仲烷基的环状或非环状溴化物均成功得到应用。该反应具有高度的化学选择性,因为酯基、酰胺基和酮基均可耐受。此方法成本低廉,且非常易于大规模实施。

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