Synthesis 2012; 44(14): 2255-2263
DOI: 10.1055/s-0032-1316540
paper
© Georg Thieme Verlag Stuttgart · New York

Regioselective Palladium(0)-Catalyzed Cross-Coupling Reactions of 5,7-Dichloro-1,6-naphthyridine

Authors

  • Iftikhar Ali

    a   Institut für Chemie, Universität Rostock, Albert Einstein Str. 3a, 18059 Rostock, Germany
  • Zahid Hassan

    a   Institut für Chemie, Universität Rostock, Albert Einstein Str. 3a, 18059 Rostock, Germany
  • Martin Hein

    a   Institut für Chemie, Universität Rostock, Albert Einstein Str. 3a, 18059 Rostock, Germany
  • Abiodun Falodun

    a   Institut für Chemie, Universität Rostock, Albert Einstein Str. 3a, 18059 Rostock, Germany
    b   Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Benin, Benin City 30001, Nigeria
  • Tamás Patonay

    c   Department of Organic Chemistry, University of Debrecen, Egyetem tér 1, 4032 Debrecen, Hungary
  • Alexander Villinger

    a   Institut für Chemie, Universität Rostock, Albert Einstein Str. 3a, 18059 Rostock, Germany
  • Peter Langer*

    a   Institut für Chemie, Universität Rostock, Albert Einstein Str. 3a, 18059 Rostock, Germany
    d   Leibniz-Institut für Katalyse an der Universität Rostock e.V., Albert Einstein Str. 29a, 18059 Rostock, Germany
Further Information

Publication History

Received: 05 February 2012

Accepted after revision: 15 May 2012

Publication Date:
26 June 2012 (online)


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Abstract

A variety of mono- and diarylated naphthyridine derivatives were prepared by site-selective Suzuki–Miyaura cross-coupling reactions of 5,7-dichloro-1,6-naphthyridine. The first attack occurs at position 5.

Supporting Information