In:
Bulletin des Sociétés Chimiques Belges, Wiley, Vol. 73, No. 5-6 ( 1964-01), p. 518-531
Abstract:
The question of the structure of the acylamidoximes is reviewed. It appears that the acylation of amidoximes invariably occurs on the oxygen atom forming O‐acyl derivatives unless the NOH group is substituted. Until now, N‐acylamidoximes have never been isolated, with the exception of the acylation products of formamidoxime. N‐acylamidoximes, however, are formed as unstable intermediates during some particular methods of synthesis of 1,2,4‐oxadiazoles. A new method of forming derivatives of this heterocycle is described.
Type of Medium:
Online Resource
ISSN:
0037-9646
,
0037-9646
DOI:
10.1002/bscb.v73:5/6
DOI:
10.1002/bscb.19640730519
Language:
English
Publisher:
Wiley
Publication Date:
1964
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