Premium
1,2,4‐Oxadiazoles. XI . An intermediate in the isomerization from nitrones to amides
Author(s) -
Baiocchi L.,
Picconi G.,
Palazzo G.
Publication year - 1979
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.5570160736
Subject(s) - chemistry , isomerization , aryl , ethanol , organic chemistry , medicinal chemistry , catalysis , alkyl
Certain 1,2,4‐oxadiazolyl‐aryl nitrones isomerize to the corresponding amides by heating in ethanol via stable intermediates, for which the structure of 1,2,4‐oxadiazolium inner salts was recognized.