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All articles of this category In a one-pot procedure 1,3,4-oxadiazoles 8 are prepared from carboxylic hydrazides 2 and keteneylidene triphenylphosphorane 1 via an untypical inter molecular Wittig olefination of a carbamate type carbonyl group. Under similar conditions, reaction of 1 and α-(hydroxyimino) carboxylic esters 9 furnishes 1,2-oxazin-6-ones 11 by a different process including an intra molecular olefination step. 1,3,4-oxadiazoles - 1,2-oxazines - phosphorus ylides - cascade reaction
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Löffler et al. (1997) studied this question.
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