4.4 Article

Copper-catalyzed decarboxylative coupling of aryl halides with alkynyl carboxylic acids performed in water

期刊

TETRAHEDRON
卷 68, 期 32, 页码 6413-6419

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2012.06.003

关键词

Coupling reactions; Alkynyl carboxylic acids; Aryl halides; Low-cost; Copper catalysis

资金

  1. International S&T Cooperation Program of Jiangsu Province [BZ2010048]
  2. Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions
  4. Key Laboratory of Organic Synthesis of Jiangsu Province

向作者/读者索取更多资源

Most alkynes are volatile liquids, which are relatively difficult to use and to transport. In contrast, alkynyl carboxylic acids offer a stable and attractive alternative for the alkynylation reactions. Here, we employed alkynyl carboxylic acids as reaction partners for the alkynylation of aryl halides. Copper-catalyzed decarboxylative coupling, including various challenging aryl bromides with phenylpropiolic acid, was performed in water without using co-solvents with good yields. Our approach provides a low-loading, low-cost, stable and environmentally friendly copper catalyst system for decarboxylative coupling. (C) 2012 Elsevier Ltd. All rights reserved.

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