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DOI: 10.1055/a-2675-3733
Enantioselective Reactions of Redox-Active Esters Catalyzed via Cooperative Photoredox/Chiral Phosphoric Acid Catalysis
Authors
This work is supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (RS-2024-00351238 and RS-2023-00259659).

Abstract
Redox-active esters have garnered significant interest owing to their bench stability and photochemical reactivity. When combined with photoredox and chiral phosphoric acid catalysis, these esters enable the formation of new carbon–carbon bonds while concurrently inducing chirality. Since the pioneering enantioselective Minisci-type addition reported by Phipps, substantial progress has been achieved in this promising field. This review summarizes the developments and mechanistic insights accumulated over the past decade, offering perspectives on future research directions.
Keywords
Asymmetric catalysis - Chiral phosphoric acid - Friedel−Crafts reaction - Minisci reaction - Photoredox catalysis - Radical reaction - Redox-active esterPublication History
Received: 20 June 2025
Accepted after revision: 03 August 2025
Accepted Manuscript online:
03 August 2025
Article published online:
22 September 2025
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