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Highly regioselective meta arylation of oxalyl amide-protected β-arylethylamine via the Catellani reaction†
Jian Han,Li Zhang,Yan Zhu,Yongxiang Zheng,Xiaolan Chen,Zhi-Bin Huang,Da-Qing Shi,Yingsheng Zhao
Chemical Communications Pub Date : 04/27/2016 00:00:00 , DOI:10.1039/C6CC02384C
Abstract

The first bidentate directing group assisted highly selective meta arylation of β-arylethylamine derivatives via palladium/norbornene catalysis is reported, and the range of aryl iodides for the oxalyl amide assisted meta-selective arylation reactions is broadest yet reported. This meta arylation also proceeds well with thiophene derivatives, giving the corresponding products in satisfactory yields. And three-step functionalization of arylethyloxalamide with three different functional groups is successfully performed.

Graphical abstract: Highly regioselective meta arylation of oxalyl amide-protected β-arylethylamine via the Catellani reaction
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