4.5 Article

The use of a bifunctional copper catalyst in the cross-coupling reactions of aryl and heteroaryl halides with terminal alkynes

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2008, Issue 23, Pages 4050-4054

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200800394

Keywords

alkynes; halides; copper; bifunctional catalysts

Funding

  1. Natural Science Foundation of Education Committee of Jiangsu Province [06KJB150099]
  2. China Postdoctoral Science Foundation
  3. Key Laboratory of Organic Synthesis of Jiangsu Province

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Copper-catalyzed cross-coupling reactions of aryl halides and heteroaryl halides with terminal alkynes were carried out in DMF at 110-130 degrees C to provide the corresponding coupling products in satisfactory-to-good yields by using inexpensive 8-hydoxyquinoline as the ligand. Noteworthy is that the bifunctional copper catalyst was successfully applied in this alkynylation reaction for the first time. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).

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