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 journalArticlepeer-review

21 Citations (Scopus)


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
Publication statusPublished - 16 Mar 2015


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

ASJC Scopus subject areas

  • Organic Chemistry

Fingerprint Dive into the research topics of 'Matsuda-Heck reaction with arenediazonium tosylates in water'. Together they form a unique fingerprint.

Cite this