Synthesis
DOI: 10.1055/a-2675-3733
Short Review

Enantioselective Reactions of Redox-Active Esters Catalyzed via Cooperative Photoredox/Chiral Phosphoric Acid Catalysis

Authors

  • Junsoo Moon

    1   School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea
  • Sujin Lee

    1   School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea
  • Eunjoo Shin

    1   School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea
  • Yongseok Kwon

    1   School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea

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).


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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.



Publication 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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