Photoannelations with α-Formyl Ketones. Enol Specificity in the Reaction of Acyclic α-Formyl Ketones with Alkenes
The irradiation of several acyclic α-formyl ketones in the presence of alkenes gives rise to photoproducts derived exclusively from that tautomer enolized toward the aldehyde carbonyl, which can then be cyclized to provide a new cyclohexenone annelation sequence. © 1975, American Chemical Society. All rights reserved.
Baldwin, SW; Gawley, RE; Doll, RJ; Leung, KH
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