Synthesis 2015; 47(12): 1726-1732
DOI: 10.1055/s-0034-1380136
paper
© Georg Thieme Verlag Stuttgart · New York

Cross-Coupling of Nonactivated Primary and Secondary Alkyl Halides with Aryl Grignard Reagents Catalyzed by Chiral Iron Pincer Complexes

Authors

  • Gerald Bauer

    Laboratory of Inorganic Synthesis and Catalysis, Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), ISIC-LSCI, BCH 3305, Lausanne 1015, Switzerland   Email: xile.hu@epfl.ch
  • Chi Wai Cheung

    Laboratory of Inorganic Synthesis and Catalysis, Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), ISIC-LSCI, BCH 3305, Lausanne 1015, Switzerland   Email: xile.hu@epfl.ch
  • Xile Hu*

    Laboratory of Inorganic Synthesis and Catalysis, Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), ISIC-LSCI, BCH 3305, Lausanne 1015, Switzerland   Email: xile.hu@epfl.ch
Further Information

Publication History

Received: 14 November 2014

Accepted: 07 January 2015

Publication Date:
11 February 2015 (online)


Graphical Abstract

Abstract

Iron(III) bisoxazolinylphenylamido (bopa) pincer complexes are efficient precatalysts for the cross-coupling of nonactivated primary and secondary alkyl halides with phenyl Grignard reagents. The reactions proceed at room temperature in moderate to excellent yields. A variety of functional groups can be tolerated. The enantioselectivity of the coupling of secondary alkyl halides is low.

Supporting Information