Walking Cations: Transition-Metal Free Benzyl Cation-Triggered sp^(2) C—H Phosphorylation and Etherification
作者机构:Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island ResourcesHainan Provincial Key Lab of Fine ChemHainan Provincial Fine Chemical Engineering Research CenterHainan UniversityHaikouHainan570228 China
出 版 物:《Chinese Journal of Chemistry》 (中国化学(英文版))
年 卷 期:2022年第40卷第24期
页 面:2933-2938页
核心收录:
学科分类:07[理学] 070303[理学-有机化学] 0703[理学-化学]
基 金:support by Hainan Provincial Natural Science Foun-dation of China(220QN180,2019RC028,2019RC129,221QN173,221QN172) Hainan University Start-up Funds(KYQD(ZR)1854 and KYQD(ZR)1857)was appreciated.
主 题:Transition metal-free Cation migration Site-selectivity Phosphorylation Etherification
摘 要:A novel benzyl cation-triggered site-selective sp^(2) C—H phosphorylation and etherification was developed. This reaction was conducted under the transition metal-free conditions through cation migration via dearomatization. Under the reaction conditions, the derivatives of naphthalenes, benzofurans and benzo[b]thiophenes all can be transformed into the corresponding products in good to excellent yields. It provides a method to construct sp^(2) C—P and sp^(2) C—O bonds as well as a new strategy for benzylic activation-triggered sp^(2) C—H functionalization.