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Photoinduced umpolung addition of carbonyl compounds with α,β-unsaturated esters enables the polysubstituted γ-lactone formation†
Jia-Yi Gu,Wei Zhang,Seth R. Jackson,Yan-Hong He,Zhi Guan
Chemical Communications Pub Date : 10/06/2020 00:00:00 , DOI:10.1039/D0CC05306F
Abstract

We herein report the photoinduced intermolecular umpolung addition of aromatic ketones/aldehydes with α,β-unsaturated esters via ketyl radical intermediates. Following an intramolecular transesterification, a variety of γ-lactone derivatives are readily accessed. Mechanistic investigations demonstrate the significant role of Hantzsch ester, which serves both as the electron and proton donor.

Graphical abstract: Photoinduced umpolung addition of carbonyl compounds with α,β-unsaturated esters enables the polysubstituted γ-lactone formation
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