Stille coupling via C–N bond cleavage

Dong-Yu Wang; Masatoshi Kawahata; Ze-Kun Yang; Kazunori Miyamoto; Shinsuke Komagawa; Kentaro Yamaguchi; Chao Wang; Masanobu Uchiyama

doi:10.1038/ncomms12937

Nature Communications (Sep 2016)

Stille coupling via C–N bond cleavage

Dong-Yu Wang,
Masatoshi Kawahata,
Ze-Kun Yang,
Kazunori Miyamoto,
Shinsuke Komagawa,
Kentaro Yamaguchi,
Chao Wang,
Masanobu Uchiyama

Affiliations

Dong-Yu Wang: Graduate School of Pharmaceutical Sciences, University of Tokyo
Masatoshi Kawahata: Faculty of Pharmaceutical Sciences at Kagawa Campus, Tokushima Bunri University
Ze-Kun Yang: Graduate School of Pharmaceutical Sciences, University of Tokyo
Kazunori Miyamoto: Graduate School of Pharmaceutical Sciences, University of Tokyo
Shinsuke Komagawa: Graduate School of Pharmaceutical Sciences, Osaka University
Kentaro Yamaguchi: Faculty of Pharmaceutical Sciences at Kagawa Campus, Tokushima Bunri University
Chao Wang: Graduate School of Pharmaceutical Sciences, University of Tokyo
Masanobu Uchiyama: Graduate School of Pharmaceutical Sciences, University of Tokyo

DOI: https://doi.org/10.1038/ncomms12937
Journal volume & issue: Vol. 7, no. 1
pp. 1 – 9

Abstract

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The Stille reaction is a long-standing method for the construction of carbon-carbon bonds by coupling aryl halides with organotin compounds. Here the authors report a Stille coupling between aryl ammonium salts and arylstannanes catalysed by nickel.

Published in Nature Communications

ISSN: 2041-1723 (Online)
Publisher: Nature Portfolio
Country of publisher: United Kingdom
LCC subjects: Science
Website: https://www.nature.com/ncomms/

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