摘要
报道了一种用简单有效的镍催化吲哚化合物和卤代氟试剂,实现吲哚2-位C—H的二氟烷基化和全氟烷基化的反应。在该催化体系中,不论是N-取代吲哚衍生物,还是N-非取代的吲哚衍生物,均可获得较高收率。初步的机理研究表明:反应归属自由基途径。
An efficient and mild Ni-catalyzed C—H difluoromethylation and perfluoroalkylation of indoles with commonly available fluoroalkyl halides has been developed.This novel transformation has demonstrated both free indole derivatives and N-substituted indole derivatives could be used to obtain the desired products in good yields.Preliminary study suggests that radical pathway was involved in the catalytic cycle.
作者
赖胤龙
张琦
张洁蓥
李健华
严绍熙
杜克斯
罗建民
LAI Yin-long;ZHANG Qi;ZHANG Jie-ying;LI Jian-hua;YAN Shao-xi;DU Ke-si;LUO Jian-min(College of Chemistry and Civil Engineering, Shaoguan University, Shaoguan 512005, China;School of Environment and Energy, South China University of Technology, Guangzhou 510640, China)
出处
《合成化学》
CAS
2021年第8期667-672,共6页
Chinese Journal of Synthetic Chemistry
基金
广东省自然科学基金面上项目(2021A1515010185)
广东省科技创新战略专项项目(“大专项+任务清单”)(韶科〔2020〕44号)
广东省普通高校科研项目(2018KQNCX236)
韶关市科技计划项目(2018sn047)。
关键词
吲哚
镍
催化
氟烷基化
N-取代
合成
机理
自由基
indole
nickel
catalysis
fluoroalkylation
N-substitution
synthesis
mechanism
radical