Abstract
The oxidation of 5-aryl-3-pyrazolidinones with mercuric oxide to the corresponding olefins is reported. Diethyl azodicarboxylate also converts 4,5-diphenyl-3-pyrazolidinone to trans-stilbene. The fragmentation of the intermediate cyclic α-carbonyl azo compounds is suggested to account for the observed products.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
13 articles.
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