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Updated: Apr 23, 2026

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Visible-light-mediated 1,2-acyl migration: the reaction of secondary enamino ketones with singlet oxygen
1Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering, and Materials Science, Soochow University, 199 RenAi Road, Suzhou, Jiangsu 215123 (China).
Abstract:
Secondary enaminones were oxidized by photochemically generated singlet oxygen, followed by nucleophilic addition of alcohol and an unexpected 1,2-acyl migration to afford quaternary amino acid derivatives. An ene-type reaction pathway is proposed. It is distinctively different from the typical [2+2] addition of singlet oxygen to a C=C bond pathway.
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