Heterocyclic Communications p. 151 - 156 (2004)
Update date:2022-08-31
Topics:
Romdhane, Anis
Gharbi, Rafik
Mighri, Zine
A new efficient route to 3,5-disubstituted-1,2,4-oxadiazoles 4a-j has been performed via the one-step reaction between arylamidoximes 1a-e and N-substituted iminoethers 2a-c. The structures of compounds 4 have been elucidated by mass spectrometry, infrared and 1H, 13C NMR measurements.
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