Features of reaction of substituted 4-oxobutanoic acids and 3H-furan-2-ones with 1,3-binucleophiles
- Authors: Grinev V.S.1,2, Amalchieva O.A.1, Egorova A.Y.1
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Affiliations:
- Saratov National State Research University named after N.G. Chernyshevsky
- Institute of Biochemistry and Physiology of Plants and Microorganisms
- Issue: Vol 53, No 11 (2017)
- Pages: 1669-1674
- Section: Article
- URL: https://journals.rcsi.science/1070-4280/article/view/216922
- DOI: https://doi.org/10.1134/S1070428017110094
- ID: 216922
Cite item
Abstract
Differences were found in reactions of 4-alkyl(aryl)-substituted 4-oxobutanoic acids and 3H-furan-2-ones with 1,3-binucleophiles, 2-(aminomethyl)aniline and 2-(aminophenyl)methanol. Depending on initial substrates different fused tricyclic systems are formed.
About the authors
V. S. Grinev
Saratov National State Research University named after N.G. Chernyshevsky; Institute of Biochemistry and Physiology of Plants and Microorganisms
Author for correspondence.
Email: grinev@ibppm.ru
Russian Federation, Astrakhanskaya ul. 83, Saratov, 410012; Saratov, 410049
O. A. Amalchieva
Saratov National State Research University named after N.G. Chernyshevsky
Email: grinev@ibppm.ru
Russian Federation, Astrakhanskaya ul. 83, Saratov, 410012
A. Yu. Egorova
Saratov National State Research University named after N.G. Chernyshevsky
Email: grinev@ibppm.ru
Russian Federation, Astrakhanskaya ul. 83, Saratov, 410012
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