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由叔烯酰胺合成含三氟甲基的异吲哚啉酮——一种串联自由基加成和环化过程。

Synthesis of trifluoromethyl-containing isoindolinones from tertiary enamides a cascade radical addition and cyclization process.

作者信息

Yu Hui, Jiao Mingdong, Fang Xiaowei, Xuan Pengfei

机构信息

School of Chemical Science and Engineering, Shanghai Key Lab of Chemical Assessment and Substainability, Tongji University 1239 Siping Road Shanghai 200092 P. R. China

出版信息

RSC Adv. 2018 Jul 3;8(42):23919-23923. doi: 10.1039/c8ra03696a. eCollection 2018 Jun 27.

Abstract

A radical trifluoromethylation reaction of tertiary enamides was investigated and trifluoromethyl-containing isoindolinones were prepared under mild conditions. Using TMSCF as a radical source, PhI(OAc) as an oxidant and KHF as an additive, tertiary enamides were converted to isoindolinones a cascade addition and cyclization process in moderate to good yields.

摘要

研究了叔烯酰胺的自由基三氟甲基化反应,并在温和条件下制备了含三氟甲基的异吲哚啉酮。以TMSCF为自由基源、PhI(OAc)为氧化剂、KHF为添加剂,叔烯酰胺通过串联加成和环化过程转化为异吲哚啉酮,产率中等至良好。

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