Email this article Acylation of Fischer’s Base with Methyl Aroylpyruvates
- Authors: Rozdyalovskaya T.A.1, Dmitriev M.V.2, Konovalova V.V.1
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Affiliations:
- Institute of Technical Chemistry, Ural Branch
- Perm National State Research University
- Issue: Vol 54, No 1 (2018)
- Pages: 139-142
- Section: Short Communications
- URL: https://journal-vniispk.ru/1070-4280/article/view/217203
- DOI: https://doi.org/10.1134/S1070428018010141
- ID: 217203
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Abstract
Methyl (Z)-4-aryl-2-hydroxy-4-oxobut-2-enoates (methyl aroylpyruvates) reacted with 1,3,3-trimethyl- 2-methylidene-2,3-dihydro-1H-indole (Fischer’s base) to give (2Z,5E)-1-aryl-3-hydroxy-5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)pent-2-ene-1,4-diones.
About the authors
T. A. Rozdyalovskaya
Institute of Technical Chemistry, Ural Branch
Email: conovalova.val@yandex.ru
Russian Federation, ul. Akad. Koroleva 3, Perm, 614013
M. V. Dmitriev
Perm National State Research University
Email: conovalova.val@yandex.ru
Russian Federation, ul. Bukireva 15, Perm, 614990
V. V. Konovalova
Institute of Technical Chemistry, Ural Branch
Author for correspondence.
Email: conovalova.val@yandex.ru
Russian Federation, ul. Akad. Koroleva 3, Perm, 614013
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