convenient Pd(0)-catalyzed carboannulation with propargylic compounds for the synthesis of highlysubstituted aromatic amine derivatives in a one-pot operation was developed. In this process, a significant breakthrough in aminobenzannulation is observed. Moreover, the reaction appears to be very general and suitable for a variety of amines.
Template Synthesis to Solve the Unreachable <i>Ortho</i> C–H Functionalization Reaction of Aryl Iodide
作者:Bo-Sheng Zhang、Wan-Yuan Jia、Yi-Ming Wang、João C. A. Oliveira、Svenja Warratz、Ze-Qiang Zhang、Xue-Ya Gou、Yong-Min Liang、Xi-Cun Wang、Zheng-Jun Quan、Lutz Ackermann
DOI:10.1021/acs.joc.3c02014
日期:2023.12.1
This report describes the use of a simple Pd/NBE catalytic system to achieve ortho C–H oxylation and phosphonylation and other functionalizations of aryliodide through templated conversion reactions. Dimethylamine is introduced in the ortho-site of aryliodide through C–H amination, and aryl dimethylamine is quickly converted to methyl quaternary ammonium salt precipitation. Methyl quaternary ammonium
[EN] PRMT5 INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS DE PRMT5 ET LEURS UTILISATIONS
申请人:EPIZYME INC
公开号:WO2015200680A2
公开(公告)日:2015-12-30
Described herein are compounds of Formula (I)-(XIII), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5-mediated disorders are also described.