First example of [3+2] cycloaddition of azomethine ylides to 5-methylidene-3-phenylhydantoin


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

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.

作者简介

M. Kukushkin

Department of Chemistry, Lomonosov Moscow State University

Email: bel@org.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

A. Kondratyeva

Department of Chemistry, Lomonosov Moscow State University

Email: bel@org.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

N. Zyk

Department of Chemistry, Lomonosov Moscow State University

Email: bel@org.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

A. Majouga

Department of Chemistry, Lomonosov Moscow State University; Mendeleev University of Chemical Technology of Russia

Email: bel@org.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991; 9 Miusskaya pl., Moscow, 125047

E. Beloglazkina

Department of Chemistry, Lomonosov Moscow State University

编辑信件的主要联系方式.
Email: bel@org.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

补充文件

附件文件
动作
1. JATS XML

版权所有 © Springer Science+Business Media, LLC, part of Springer Nature, 2019