Photochemical rearrangement of 2-(N-allyl-N-alkylamino)cyclohex-2-enones

DOI: 10.1002/recl.19951141113

Source and publish data:

Recueil des Travaux Chimiques des Pays-Bas p. 492 - 497 (1995)

Update date:2022-08-03

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Authors:

Meyer, Catherine

Pete, Jean-Pierre

Piva, Olivier

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Article abstract of DOI:10.1002/recl.19951141113

Irradiation at 366 nm of 2-(N-allyl-N-alkylamino)cyclohex-2-enones led, surprisingly, to very unstable 1-azaspiro<2.5>octan-4-ones rather than to the expected <2 + 2> intramolecular photocycloaddition.The corresponding alcohols could be isolated in good y

Full text of DOI:10.1002/recl.19951141113

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