Synthesis and reactivity of carbazole-containing hypervalent iodine(Ⅲ) reagents  

作　　者：Tianlei Lan Haijuan Qin Wenting Chen Wei Liu Chao Chen 

机构地区：[1]College of Science,College of Chemical Engineering and Materials Science,Centre of Modern Analytical Technology,Tianjin University of Science and Technology,Tianjin 300457,China [2]Key Laboratory of Bioorganic Phosphorus Chemistry&Chemical Biology(Ministry of Education,MOE),Department of Chemistry,Tsinghua University,Beijing 100084 China [3]Beijing Laviana Pharmatech Co.,Ltd.,Beijing 102206,China

出　　处：《Chinese Chemical Letters》2020年第2期357-360,共4页中国化学快报（英文版）

基　　金：supported by the National Key Research and Development Program of China(No.2016YFB0401400);the National Natural Science Foundation of China(Nos.21302139,21672120 and 21871158);the Fok Ying Tong Education Foundation of China(No.151014)。

摘　　要：A range of bench-stable carbazole-containing hypervalent iodine(Ⅲ) reagents were synthesized by I-N bond formation in good yields.This kind of benziodoxolone reagents was used for a C-N coupling reaction to introduce a carbazole group to aromatic heterocycle compounds.A range of bench-stable carbazole-containing hypervalent iodine(Ⅲ) reagents were synthesized by I-N bond formation in good yields.This kind of benziodoxolone reagents was used for a C-N coupling reaction to introduce a carbazole group to aromatic heterocycle compounds.

关 键 词：CARBAZOLES Hypervalentiodine REAGENTS Benziodoxolones N-ARYLATION THIOPHENES 

分 类 号：TQ421[化学工程]