FORMATION OF 1,2-OXAZINE DERIVATIVES: A NOVEL TYPE OF REACTION BETWEEN 2-AMINOOXAZOLES AND MALEIC ACID IMIDE

Authors

  • Г. Я. Кондратьева N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow
  • M. А. Айтжaнова N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow
  • B. C. Богданов N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow
  • Г. А. Сташина N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow
  • И. П. Седишев N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow

DOI:

https://doi.org/10.1007/302

Keywords:

2-aminooxazoles, 3-(2-aza-1-amino-3-methyl-4-oxopenten-2-ylidene)-2, 5-dioxopyrrolidines, N, N-dimethylamides of 3, 4-disubstituted 5, 6-hydropyrrolo[3, 2-e]-1, 2-oxazine-2-carboxylic acids, maleinimide

Abstract

N,N-Disubstituted 2-aminooxazoles in acetic acid at 20°C undergo addition of maleinimide, converting to alkylidene succinimides or 1,2-oxazine derivatives.

Authors: G. Ya. Kondrat'eva, M. A. Aitzhanova, V. S. Bogdanov, G. A. Stashina, and I. P. Sedishev.

English Translation in Chemistry of Heterocyclic Compounds, 2000, 36 (8), pp 989-992

http://link.springer.com/article/10.1007/BF02256987

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Published

2013-02-12

Issue

No. 8 (2000)

Section

Original Papers