SYNTHESIS OF 3-SUBSTITUTED 2-AMINO-1-HYDROXY-1<i>H</i>-INDOLE-5,6-DICARBONITRILES

Authors

  • С. И. Филимонов Yaroslavl State Technical University
  • Ж. В. Чиркова Yaroslavl State Technical University
  • В. С. Шарунов Yaroslavl State Technical University
  • И. Г. Абрамов Yaroslavl State Technical University
  • Г. А. Сташина N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
  • С. И. Фирганг N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
  • К. Ю. Супоницкий A. N. Nesmeyanov Institute of Organoelement Compounds

DOI:

https://doi.org/10.1007/1231

Keywords:

2, 1-benzisoxazoles, 1-hydroxy-1H-indole-5, 6-dicarbonitriles, phthalonitriles, C-nucleophilic substitution, reductive cyclization

Abstract

A method of synthesizing new 3-substituted 2-amino-1-hydroxy-1H-indole-5,6-dicarbonitriles has been developed based on the reductive cyclization of substituted 4-cyanomethyl-5-nitrophthalonitriles.

Authors: S. I. Filimonov, Zh. V. Chirkova, V. S. Sharunov, I. G. Abramov, G. A. Stashina, S. I. Firgang, and K. Yu. Suponitsky.

English Translation in Chemistry of Heterocyclic Compounds, 2012, 48 (3), pp 427-435

http://link.springer.com/article/10.1007/s10593-012-1010-6

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Published

2013-11-25

Issue

No. 3 (2012)

Section

Original Papers