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机构地区:[1]Chemistry Department,School of Science,Tianjin University,Tianjin 300072,China [2]Chemistry and Pharmaceutical Engineering College,Nanyang Normal University,Nanyang,Henan 473061,China
出 处:《Chinese Journal of Chemistry》2012年第10期2389-2393,共5页中国化学(英文版)
基 金:This work was supported by the National Natural Science Foundation of China (No. 20802049).
摘 要:A simple and efficient C--N cross-coupling method of aryl halides with various heterocycles was reported, by using 10 tool% of CuI as catalyst and 1.2 equiv. Nail as base. Aryl iodides, aryl bromides and many substituted atyl chlorides could efficiently react with heterocycles, providing variety of N-arylated products in good to excellent yields. The ligand-free catalyst system was stable in air and could be readily reused.A simple and efficient C--N cross-coupling method of aryl halides with various heterocycles was reported, by using 10 tool% of CuI as catalyst and 1.2 equiv. Nail as base. Aryl iodides, aryl bromides and many substituted atyl chlorides could efficiently react with heterocycles, providing variety of N-arylated products in good to excellent yields. The ligand-free catalyst system was stable in air and could be readily reused.
关 键 词:N-ARYLATION aryl halide HETEROCYCLE CROSS-COUPLING CUI
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