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Oximes as products in the reactions of 5‐substituted 2‐nitrothiophenes with arylacetonitriles
Author(s) -
Rad Nazar I.,
Teslenko Yuriy O.,
Obushak Mykola D.,
Matiychuk Vasyl S.,
Lytvyn Roman Z.
Publication year - 2011
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.723
Subject(s) - chemistry , acetonitriles , isoxazole , potassium hydroxide , methanol , aryl , medicinal chemistry , organic chemistry , acetonitrile , alkyl
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)‐thienylidene](aryl)acetonitriles. Under proposed reaction conditions, the formation of thieno[2,3‐ c ]isoxazole was not the case. J. Heterocyclic Chem., (2011).
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