Trisubstituted oxazoles I react at −15° with singlet oxygen to give dioxazoles III and iminoanhydrides V which rearrange at room temperature to triamides VI. The intermediate ratio (III/V) is sensitive to the reaction temperature. It is likely that at room temperature triamides VI are essentially formed via imino‐anhydrides V. Copyright © 1978 Journal of Heterocyclic Chemistry

Intermediates in the reaction of singlet oxygen with trisubstituted oxazoles / Graziano, M. L.; Iesce, M. R.; Scarpati, R.. - In: JOURNAL OF HETEROCYCLIC CHEMISTRY. - ISSN 0022-152X. - 15:7(1978), pp. 1205-1207. [10.1002/jhet.5570150725]

Intermediates in the reaction of singlet oxygen with trisubstituted oxazoles

Graziano M. L.;Iesce M. R.;
1978

Abstract

Trisubstituted oxazoles I react at −15° with singlet oxygen to give dioxazoles III and iminoanhydrides V which rearrange at room temperature to triamides VI. The intermediate ratio (III/V) is sensitive to the reaction temperature. It is likely that at room temperature triamides VI are essentially formed via imino‐anhydrides V. Copyright © 1978 Journal of Heterocyclic Chemistry
1978
Intermediates in the reaction of singlet oxygen with trisubstituted oxazoles / Graziano, M. L.; Iesce, M. R.; Scarpati, R.. - In: JOURNAL OF HETEROCYCLIC CHEMISTRY. - ISSN 0022-152X. - 15:7(1978), pp. 1205-1207. [10.1002/jhet.5570150725]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/858139
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