Email this article First example of [3+2] cycloaddition of azomethine ylides to 5-methylidene-3-phenylhydantoin
- Authors: Kukushkin M.E.1, Kondratyeva A.A.1, Zyk N.V.1, Majouga A.G.1,2, Beloglazkina E.K.1
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Affiliations:
- Department of Chemistry, Lomonosov Moscow State University
- Mendeleev University of Chemical Technology of Russia
- Issue: Vol 68, No 11 (2019)
- Pages: 2088-2091
- Section: Full Articles
- URL: https://ogarev-online.ru/1066-5285/article/view/243531
- DOI: https://doi.org/10.1007/s11172-019-2670-5
- ID: 243531
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Abstract
New type dispiroindolinones, dispiroimidazolidine-4,3′-pyrrolidine-2′,3″-indolinones unsubstituted at position 4′ of the central pyrrolidine ring, were synthesized by the 1,3-dipolar cycloaddition of azomethine ylides, generated from N-alkyl-substituted amino acids and isatines, to 5-methylidene-substituted 3-phenylhydantoin.
About the authors
M. E. Kukushkin
Department of Chemistry, Lomonosov Moscow State University
Email: bel@org.chem.msu.ru
Russian Federation, Build. 3, 1 Leninskie Gory, Moscow, 119991
A. A. Kondratyeva
Department of Chemistry, Lomonosov Moscow State University
Email: bel@org.chem.msu.ru
Russian Federation, Build. 3, 1 Leninskie Gory, Moscow, 119991
N. V. Zyk
Department of Chemistry, Lomonosov Moscow State University
Email: bel@org.chem.msu.ru
Russian Federation, Build. 3, 1 Leninskie Gory, Moscow, 119991
A. G. Majouga
Department of Chemistry, Lomonosov Moscow State University; Mendeleev University of Chemical Technology of Russia
Email: bel@org.chem.msu.ru
Russian Federation, Build. 3, 1 Leninskie Gory, Moscow, 119991; 9 Miusskaya pl., Moscow, 125047
E. K. Beloglazkina
Department of Chemistry, Lomonosov Moscow State University
Author for correspondence.
Email: bel@org.chem.msu.ru
Russian Federation, Build. 3, 1 Leninskie Gory, Moscow, 119991
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