Application of Bifunctional Togni’s Reagent in Photoredox‐Catalyzed Oxytrifluoromethylation of Alkenes
Year: 2026
Type: article
Abstract: We report a radical‐based protocol for the photoredox‐catalyzed oxytrifluoromethylation of alkenes with Togni’s reagent. This strategy provides efficient access to a broad array of CF 3 ‐containing esters and is also applicable to late‐stage functionalization of drug molecules under mild conditions. Moreover, conversion of the resulting CF 3 ‐functionalized esters to other valuable building blocks is also achieved. Mechanistic investigations reveal that Togni’s reagent acts as both a trifluoromethyl and an acyloxy group. Consequently, the difunctionalization reaction can proceed without any external nucleophiles, offering high atom economy.
Source: Advanced Synthesis & Catalysis
DOI: 10.1002/adsc.70844
Institution: Xinyang Normal University
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: bronze
OpenAlex ID: W7224552626
