Oxidation by ground‐state molecular oxygen of fully substituted alkoxyoxazoles I gave imines IV as major products; diacylcarbamates III were also obtained as minor products. The free radical nature of the autoxidation was established. A mechanistic interpretation of the results is suggested also in the light of the results of the oxidation with singlet oxygen. Copyright © 1977 Journal of Heterocyclic Chemistry

Comparison between triplet and singlet molecular oxygen oxidation of fully substituted alkoxyoxazoles

Graziano M. L.;Iesce M. R.;
1977

Abstract

Oxidation by ground‐state molecular oxygen of fully substituted alkoxyoxazoles I gave imines IV as major products; diacylcarbamates III were also obtained as minor products. The free radical nature of the autoxidation was established. A mechanistic interpretation of the results is suggested also in the light of the results of the oxidation with singlet oxygen. Copyright © 1977 Journal of Heterocyclic Chemistry
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/858136
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