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 |
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Pages (from-to) | 358-362 |
Number of pages | 5 |
Journal | Beilstein Journal of Organic Chemistry |
Volume | 11 |
DOIs | |
Publication status | Published - 16 Mar 2015 |
Keywords
- Alkyl cinnamates
- Diazonium salts
- Matsuda-Heck reaction
- Microwave-assisted synthesis
- Stilbenes
ASJC Scopus subject areas
- Organic Chemistry