化学
芳基
叠氮化钠
催化作用
铜
叠氮化物
钠
组合化学
有机化学
药物化学
烷基
作者
Satish R. Lanke,Bhalchandra M. Bhanage
标识
DOI:10.1080/00397911.2013.808349
摘要
Abstract Abstract This work reports an efficient protocol for the coupling reaction of aryl iodides/boronic acids with sodium azide to aryl azides/amines in the presence of copper bis(2,2,6,6-tetramethyl-3,5-heptanedionate) Cu(TMHD)2 catalyst. The Cu(TMHD)2 catalyst is a structurally well-defined, O-containing, air- and moisture-stable, transition-metal complex and works at mild reaction conditions. It was observed that aryl azides can be reduced further to corresponding aniline derivatives using the same catalyst under basic reaction conditions for a prolonged period. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.] GRAPHICAL ABSTRACT Keywords: Aminesaryl iodidesazidationboronic acidcopper ACKNOWLEDGMENT S. R. L. is thankful to the Department of Atomic Energy (ICT-DAE Centre), Mumbai, India, for a senior research fellowship.
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