Abstract
Abstract Azide was prepared from the corresponding acid chloride . The base catalyzed decomposition with aromatic amines, aminobenzoic acids and/or hydrazines afforded the corresponding anilides and/or hydrazides via azido group displacement. Compounds and were refluxed in Ac2O to give 1,3,4-oxadiazole derivatives and . Lewis acid catalyzed decomposition of azide with anhyd. AlCl3 in dry aromatic substrates gave the corresponding ketones . Also, the reaction of azide with glycine gave .
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