Photoredox-Catalyzed Transfer Thiobenzoyloxylation of Styrenes Using Oxime-Based Surrogates

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.

Authors

Sergiu Bicic (ORCID: https://orcid.org/0009-0006-4245-9057)
Martin Oestreich

Institutions

Technische Universität Berlin (DE)

Publication Details

Journal: Synthesis
Published: 2026-02-04
DOI: https://doi.org/10.1055/a-2804-6947
Primary Topic: Sulfur-Based Synthesis Techniques
Type: article
Field-Weighted Citation Impact: 0.00

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article

Photoredox-Catalyzed Transfer Thiobenzoyloxylation of Styrenes Using Oxime-Based Surrogates

Sergiu Bicic, Martin Oestreich

Feb 4, 2026

Synthesis

Sulfur-Based Synthesis Techniques

article

Photoredox-Catalyzed Transfer Thiobenzoyloxylation of Styrenes Using Oxime-Based Surrogates

Sergiu Bicic, Martin Oestreich

February 4, 2026article en

Abstract

Synthesis

Technische Universität Berlin (DE)

Openalex Percentile: Top 66%

Sulfur-Based Synthesis Techniques

DOI Source OpenAlex

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Photoredox-Catalyzed Transfer Thiobenzoyloxylation of Styrenes Using Oxime-Based Surrogates — Sergiu Bicic, Martin Oestreich · Synthesis (2026) | TGRS Research Map | TGRS