Synthesis 2017; 49(24): 5396-5412
DOI: 10.1055/s-0036-1589101
paper
© Georg Thieme Verlag Stuttgart · New York

Nickel-Catalyzed Cross-Coupling of Functionalized Organo­manganese Reagents with Aryl and Heteroaryl Halides Promoted by 4-Fluorostyrene

Andreas D. Benischke
a   Department of Chemistry, Ludwig-Maximilians-Universität München, Butenandtstr. 5–13, 81377 München, Germany   Paul.Knochel@cup.uni-muenchen.de
,
Alexandre Desaintjean
b   Institut de Recherche de Chimie Paris, CNRS, Chimie Paris Tech, 11 Rue Pierre et Marie Curie, 75005 Paris, France   Email: gerard.cahiez@chimie-paristech.fr
,
Thomas Juli
a   Department of Chemistry, Ludwig-Maximilians-Universität München, Butenandtstr. 5–13, 81377 München, Germany   Paul.Knochel@cup.uni-muenchen.de
,
Gérard Cahiez
b   Institut de Recherche de Chimie Paris, CNRS, Chimie Paris Tech, 11 Rue Pierre et Marie Curie, 75005 Paris, France   Email: gerard.cahiez@chimie-paristech.fr
,
a   Department of Chemistry, Ludwig-Maximilians-Universität München, Butenandtstr. 5–13, 81377 München, Germany   Paul.Knochel@cup.uni-muenchen.de
› Author Affiliations
Further Information

Publication History

Received: 25 July 2017

Accepted after revision: 03 August 2017

Publication Date:
30 August 2017 (online)


Abstract

A catalytic system consisting of Ni(acac)2 (5 mol%) and 4-fluorostyrene (20 mol%) allows a convenient cross-coupling of functionalized organomanganese reagents with a variety of aryl and heteroaryl halides leading to polyfunctionalized diaryl- and arylheteroarylmethane derivatives.

Supporting Information

 
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