College of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai 210032, China.
Org Biomol Chem. 2011 Dec 21;9(24):8224-7. doi: 10.1039/c1ob06208e. Epub 2011 Oct 11.
Under the catalysis of CuI/2-carboxylic acid-quinoline-N-oxide, the cross coupling reactions between aryl iodides or bromides and aqueous ammonia proceed very well to afford N-unprotected aniline derivatives in excellent yields. This inexpensive catalytic system shows great functional group tolerance and excellent reaction selectivity.
在 CuI/2-羧酸-喹啉-N-氧化物的催化下,芳基碘化物或溴化物与氨水溶液的交叉偶联反应非常顺利,以优异的收率得到了未保护的苯胺衍生物。该廉价的催化体系显示出了很好的官能团容忍性和优异的反应选择性。