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通过钯催化将苄醇直接交叉偶联以构建二芳基甲烷。

Direct cross-coupling of benzyl alcohols to construct diarylmethanes via palladium catalysis.

作者信息

Cao Zhi-Chao, Yu Da-Gang, Zhu Ru-Yi, Wei Jiang-Bo, Shi Zhang-Jie

机构信息

Beijing National Laboratory of Molecule Science (BNLMS) and Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry and Green Chemistry Center, Peking University, Beijing, 100871, China.

出版信息

Chem Commun (Camb). 2015 Feb 14;51(13):2683-6. doi: 10.1039/c4cc10084k.

Abstract

A direct arylation to furnish diarylmethanes from benzyl alcohols was realized through Pd(PPh3)4-catalyzed Suzuki-Miyaura coupling via benzylic C-O activation in the absence of any additives. The arylation is compatible with various functional groups. This development provides an atom- and step-economic way to approach a diarylmethane scaffold under mild and environmentally benign conditions.

摘要

在无任何添加剂的情况下,通过钯(四三苯基膦)催化的铃木-宫浦偶联反应,经由苄基碳-氧活化,实现了从苄醇直接芳基化制备二芳基甲烷。该芳基化反应与多种官能团兼容。此进展提供了一种原子经济和步骤经济的方法,可在温和且环境友好的条件下构建二芳基甲烷骨架。

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