Journal of the Chemical Society. Chemical communications p. 202 - 204 (1981)
Update date:2022-07-29
Topics:
Takeuchi, Hiroshi
Koyama, Kikuhiko
The photolysis and thermolysis of phenyl azide in acetic acid gave 2,3-dihydro-1H-azepin-2-one via 1-azacyclohepta-1,2,4,6-tetraene, and ring-disubstituted products via a resonance-stabilized ion formed by attack of singlet phenylnitrene on acetic acid.
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