Matsuda-Heck reaction with arenediazonium tosylates in water

Ksenia V. Kutonova, Marina E. Trusova, Andrey V. Stankevich, Pavel S. Postnikov, Victor D. Filimonov

Research output: Contribution to journal › Article

Abstract

An environmentally friendly Matsuda-Heck reaction with arenediazonium tosylates has been developed for the first time. A range of alkenes was arylated in good to quantitative yields in water. The reaction is significantly accelerated when carried out under microwave heating. The arylation of haloalkylacrylates with diazonium salts has been implemented for the first time.

Original language	English
Pages (from-to)	358-362
Number of pages	5
Journal	Beilstein Journal of Organic Chemistry
Volume	11
DOIs	https://doi.org/10.3762/bjoc.11.41
Publication status	Published - 16 Mar 2015

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Keywords

Alkyl cinnamates
Diazonium salts
Matsuda-Heck reaction
Microwave-assisted synthesis
Stilbenes

ASJC Scopus subject areas

Organic Chemistry

Cite this

Kutonova, K. V., Trusova, M. E., Stankevich, A. V., Postnikov, P. S., & Filimonov, V. D. (2015). Matsuda-Heck reaction with arenediazonium tosylates in water. Beilstein Journal of Organic Chemistry, 11, 358-362. https://doi.org/10.3762/bjoc.11.41

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AU - Postnikov, Pavel S.

AU - Filimonov, Victor D.

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Access to Document

10.3762/bjoc.11.41