Synthesis 2015; 47(17): 2641-2646
DOI: 10.1055/s-0034-1380752
paper
© Georg Thieme Verlag Stuttgart · New York

Palladium-Catalyzed Carbonylative Synthesis of N-Benzoylindoles with Mo(CO)6 as the Carbon Monoxide Source

Authors

  • Xiao-Feng Wu*

    a   Department of Chemistry, Zhejiang Sci-Tech University, Xiasha Campus, Hangzhou Province, P. R. of China   Email: xiao-feng.wu@catalysis.de
    b   Leibniz-Institut für Katalyse e.V. an der Universität Rostock, Albert-Einstein-Str. 29a, 18059 Rostock, Germany
  • Stefan Oschatz

    b   Leibniz-Institut für Katalyse e.V. an der Universität Rostock, Albert-Einstein-Str. 29a, 18059 Rostock, Germany
    c   Universität Rostock, Institut für Chemie, Albert-Einstein-Str. 3a, 18059 Rostock, Germany   Email: peter.langer@uni-rostock.de
  • Muhammad Sharif

    b   Leibniz-Institut für Katalyse e.V. an der Universität Rostock, Albert-Einstein-Str. 29a, 18059 Rostock, Germany
  • Peter Langer*

    b   Leibniz-Institut für Katalyse e.V. an der Universität Rostock, Albert-Einstein-Str. 29a, 18059 Rostock, Germany
    c   Universität Rostock, Institut für Chemie, Albert-Einstein-Str. 3a, 18059 Rostock, Germany   Email: peter.langer@uni-rostock.de
Further Information

Publication History

Received: 12 February 2015

Accepted after revision: 16 April 2015

Publication Date:
28 May 2015 (online)


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Abstract

A mild and carbon monoxide gas-free palladium-catalyzed aminocarbonylation of indole has been developed for the synthesis of N-benzoylindoles. This method uses Mo(CO)6 as a convenient CO-precursor and BuPAd2 as the ligand. A number of substituents on the aryl bromide species is tolerated under the presented conditions and gave the desired products in up to excellent yields.

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