Ammonium Salt-Catalyzed Highly Practical <i>Ortho</i>-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
作者:Xiaodong Xiong、Ying-Yeung Yeung
DOI:10.1021/acscatal.8b00327
日期:2018.5.4
An ortho-selective ammonium chloride salt-catalyzed direct C–H monohalogenation of phenols and 1,1′-bi-2-naphthol (BINOL) with 1,3-dichloro-5,5-dimethylhydantoin (DCDMH) as the chlorinating agent has been developed. The catalyst loading was low (down to 0.01 mol %) and the reaction conditions were very mild. A wide range of substrates including BINOLs were compatible with this catalytic protocol. Chlorinated
Direct sulfenylation and selenylation of phenols using a stoichiometric amount of FeCl3 under an oxygen atmosphere has been developed. The chalcogenated phenols were shown to be suitable for preparing S- and Se-containing compounds using the reaction of the remaining hydroxy group.