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由铁(III)醇盐-N-杂环卡宾催化剂体系实现的选择性熊田联芳基交叉偶联反应。

Selective Kumada biaryl cross-coupling reaction enabled by an iron(III) alkoxide-N-heterocyclic carbene catalyst system.

作者信息

Chua Yi-Yuan, Duong Hung A

机构信息

Institute of Chemical and Engineering Sciences (ICES), Agency for Science, Technology and Research (A*STAR), 8, Biomedical Grove, Neuros, #07-01, Singapore 138665.

出版信息

Chem Commun (Camb). 2014 Aug 7;50(61):8424-7. doi: 10.1039/c4cc02930e.

DOI:10.1039/c4cc02930e
PMID:24947849
Abstract

A catalyst system comprising Fe2(O(t)Bu)6 and an N-heterocyclic carbene ligand enables efficient syntheses of (hetero)biaryls from the reactions of aryl Grignard reagents with a diverse spectrum of (hetero)aryl chlorides. Amongst the alkoxide and amide counterions investigated, tert-butoxide was the most effective in inhibiting the homocoupling of arylmagnesiums.

摘要

一种由Fe2(O(t)Bu)6和一种氮杂环卡宾配体组成的催化剂体系,能够使芳基格氏试剂与多种(杂)芳基氯化物反应高效合成(杂)联芳基。在所研究的醇盐和酰胺抗衡离子中,叔丁醇盐在抑制芳基镁的均偶联方面最为有效。

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