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 journalArticle

19 Citations (Scopus)

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 languageEnglish
Pages (from-to)358-362
Number of pages5
JournalBeilstein Journal of Organic Chemistry
Volume11
DOIs
Publication statusPublished - 16 Mar 2015

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Microwave heating
Alkenes
Salts
Water

Keywords

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

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Matsuda-Heck reaction with arenediazonium tosylates in water. / Kutonova, Ksenia V.; Trusova, Marina E.; Stankevich, Andrey V.; Postnikov, Pavel S.; Filimonov, Victor D.

In: Beilstein Journal of Organic Chemistry, Vol. 11, 16.03.2015, p. 358-362.

Research output: Contribution to journalArticle

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AU - Filimonov, Victor D.

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