区域选择性
化学
烯丙基重排
三氟甲基
催化作用
镍
烯烃
有机化学
构造(python库)
组合化学
药物化学
烷基
计算机科学
程序设计语言
作者
Qingqing Zhang,Ruo‐Xing Jin,Qian Gao,Peng Liu,Ya-Wen Zuo,Quan Lan,Xi‐Sheng Wang
标识
DOI:10.1021/acs.orglett.5c00980
摘要
Introducing fluorine atoms or fluorine-containing groups into drug molecules has become a common approach in drug design, with the incorporation of trifluoromethyl groups as a focal point of research in the field of organic fluorochemistry. Here, we describe a nickel-catalyzed hydrotrifluoromethylation of internal alkynes with trifluoromethyl alkyl bromides to synthesize a series of highly regioselective trifluoromethyl allyl trisubstituted alkenes. This reaction is characterized by mild conditions and broad functional-group tolerance, providing an efficient and practical approach to synthesize trifluoromethyl allyl trisubstituted alkenes.
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