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Synthesis
DOI: 10.1055/a-2804-6947
DOI: 10.1055/a-2804-6947
Paper
Photoredox-Catalyzed Transfer Thiobenzoyloxylation of Styrenes Using Oxime-Based Surrogates
Authors
This research was supported by the Deutsche Forschungsge-meinschaft (Oe 249/26-1). M.O. is indebted to the Einstein Foundation Berlin for an endowed professorship.
Supported by: Deutsche Forschungsgemeinschaft Oe 249/26-1

Abstract
Based on our previous work, a photoredox-catalyzed transfer thiobenzoyloxylation of styrenes using oxime-based surrogates is reported. The redox-neutral protocol enables regioselective vicinal C–S and C–O bond formation under mild conditions. Mechanistic studies support a radical–polar crossover pathway.
Keywords
Difunctionalization - Oximes - Photoredox catalysis - Single electron transfer - Transfer reactionsPublication History
Received: 16 January 2026
Accepted after revision: 04 February 2026
Accepted Manuscript online:
04 February 2026
Article published online:
17 February 2026
© 2026. Thieme. All rights reserved.
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For reviews on vicinal 1,2-difunctionalization of alkenes, see:
For reviews on photocatalyzed difunctionalization of alkenes, see:
For recent reviews on transfer functionalization reactions, see:
For reviews on oxysulfenylation strategies, see:
For recent articles on oxysulfenylation reactions, see: