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作 者:Jian Xu Zhijie Kuang Qiuling Song
出 处:《Chinese Chemical Letters》2018年第6期963-966,共4页中国化学快报(英文版)
基 金:Financial support from the Recruitment Program of Global Experts (1000 Talents Plan);the Natural Science Foundation of Fujian Province (No. 2016J01064);Fujian Hundred Talents Plan, Program of Innovative Research Team of Huaqiao University (No. Z14X0047);Subsidized Project for Cultivating Postgraduates’ Innovative Ability in Scientific Research of Huaqiao University (for Z. Kuang) are gratefully acknowledged
摘 要:An expedient and mild strategy for the synthesis of unconventional 2-(dimethylamino)-3,3-difluorochroman-4-one derivatives from o-hydroxyarylenaminones and Selectfluor was developed at room temperature under catalyst-free conditions. This method showed excellent chemoselectivity and great functional groups tolerance.An expedient and mild strategy for the synthesis of unconventional 2-(dimethylamino)-3,3-difluorochroman-4-one derivatives from o-hydroxyarylenaminones and Selectfluor was developed at room temperature under catalyst-free conditions. This method showed excellent chemoselectivity and great functional groups tolerance.
关 键 词:SELECTFLUOR o-Hydroxyarylenaminones CATALYST-FREE Chroman-4-one Fluorination reaction Fluorine-contained compound
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