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Nickel-Catalyzed Heck-Type Monofluoroacetation of Styrenes for Facile Synthesis of Allylic Fluorides.

作者信息

Wang Zhen-Yu, Wan Jia-Hao, Wang Gao-Yin, Jin Ruo-Xing, Lan Quan, Wang Xi-Sheng

机构信息

Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry, University of Science and Technology of China, Hefei, Anhui, 230026, P.R. China.

出版信息

Chem Asian J. 2018 Feb 2;13(3):261-265. doi: 10.1002/asia.201701655. Epub 2018 Jan 17.

DOI:10.1002/asia.201701655
PMID:29266780
Abstract

An efficient nickel-catalyzed Heck-type reaction between styrenes and fluoroalkyl iodine has been developed. This novel transformation has demonstrated a broad substrate scope, mild reaction conditions and excellent E-stereoselectivity. This efficient synthetic method has been applied to the late-stage monofluoroacetation of biologically active molecules. Mechanistic investigations indicate that a monofluoroalkyl radical is involved in the catalytic cycle.

摘要

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