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Oximes as products in the reactions of 5-substituted 2-nitrothiophenes with arylacetonitriles

✍ Scribed by Nazar I. Rad; Yuriy O. Teslenko; Mykola D. Obushak; Vasyl S. Matiychuk; Roman Z. Lytvyn

Publisher
Journal of Heterocyclic Chemistry
Year
2011
Tongue
English
Weight
76 KB
Volume
48
Category
Article
ISSN
0022-152X

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✦ Synopsis

Abstract

It has been shown that reactions 5‐substituted 2‐nitrothiophenes with arylacetonitriles in the presence of potassium hydroxide in methanol lead to the formation of the new 2‐(hydroxyimino)‐5‐R‐3(2H)‐thienylideneacetonitriles. Under proposed reaction conditions, the formation of thieno[2,3‐c]isoxazole was not the case. J. Heterocyclic Chem., (2011).

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