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 | |
| 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
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 journal › Article
}
TY - JOUR
T1 - Matsuda-Heck reaction with arenediazonium tosylates in water
AU - Kutonova, Ksenia V.
AU - Trusova, Marina E.
AU - Stankevich, Andrey V.
AU - Postnikov, Pavel S.
AU - Filimonov, Victor D.
PY - 2015/3/16
Y1 - 2015/3/16
N2 - 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.
AB - 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.
KW - Alkyl cinnamates
KW - Diazonium salts
KW - Matsuda-Heck reaction
KW - Microwave-assisted synthesis
KW - Stilbenes
UR - http://www.scopus.com/inward/record.url?scp=84934874301&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84934874301&partnerID=8YFLogxK
U2 - 10.3762/bjoc.11.41
DO - 10.3762/bjoc.11.41
M3 - Article
VL - 11
SP - 358
EP - 362
JO - Beilstein Journal of Organic Chemistry
JF - Beilstein Journal of Organic Chemistry
SN - 1860-5397
ER -