Oxidation of reaction products of p-aryl-С,С-disubstituted nitrones and dimethyl 3-methylenecyclopropane-1,2-dicarboxylate
- Authors: Molchanov A.P.1, Tran T.Q.2, Stepakov A.V.1, Kostikov R.R.1
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Affiliations:
- St. Petersburg State University
- School of Chemical Engineering
- Issue: Vol 52, No 11 (2016)
- Pages: 1603-1605
- Section: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/215210
- DOI: https://doi.org/10.1134/S1070428016110099
- ID: 215210
Cite item
Abstract
Oxidation with 2,3-dichloro-4,5-dicyanobenzoquinone of 2,4-dihydro-1Н-azeto[1,2-a]quinoline-3,4 -dicarboxylates obtained in the reaction of N-aryl-С,С-disubstituted nitrones with Feist’s acid ester resulted in the formation of 2-vinylquinoline-3,4-dicarboxylates in good yields.
About the authors
A. P. Molchanov
St. Petersburg State University
Author for correspondence.
Email: a.molchanov@spbu.ru
Russian Federation, Universitetskaya nab. 7/9, St. Petersburg, 199034
T. Q. Tran
School of Chemical Engineering
Email: a.molchanov@spbu.ru
Viet Nam, Hanoi
A. V. Stepakov
St. Petersburg State University
Email: a.molchanov@spbu.ru
Russian Federation, Universitetskaya nab. 7/9, St. Petersburg, 199034
R. R. Kostikov
St. Petersburg State University
Email: a.molchanov@spbu.ru
Russian Federation, Universitetskaya nab. 7/9, St. Petersburg, 199034
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