Metal-Free Reagents and Catalysts for C–C Multiple Bond Reduction

Abstract Organic reductants are increasingly important for the reduction of C–C multiple bonds, as they avoid scarce platinum-group metals and broadly tolerate Lewis-basic motifs common in medicinal chemistry. Diverse reduction mechanism via hydride transfer, protonation, hydroboration, frustrated Lewis pair-mediated H₂ activation, diimide-mediated hydrogen transfer, and photoinduced electron, energy, or hydrogen atom transfer provide distinct and often complementary reactivity orders enabling predictable reductions even in complex molecules. This review discusses the main mechanisms and categorizes them based on the reducible substrate classes and the tolerance of Lewis-basic motifs, highlighting methods with particular relevance to medicinal chemistry applications.

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Publication Details

Journal
Synthesis
Published
2025-11-26
DOI
https://doi.org/10.1055/a-2742-1904
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
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article

Metal-Free Reagents and Catalysts for C–C Multiple Bond Reduction

Dang H. Vu, Benjamin R. G. Bissinger, Mario P. Wiesenfeldt, Kirti Devi et al.
Synthesis
Radical Photochemical Reactions
article

Metal-Free Reagents and Catalysts for C–C Multiple Bond Reduction

Dang H. Vu, Benjamin R. G. Bissinger, Mario P. Wiesenfeldt, Kirti Devi, Asad Shehzad
article en

Abstract

Abstract Organic reductants are increasingly important for the reduction of C–C multiple bonds, as they avoid scarce platinum-group metals and broadly tolerate Lewis-basic motifs common in medicinal chemistry. Diverse reduction mechanism via hydride transfer, protonation, hydroboration, frustrated Lewis pair-mediated H₂ activation, diimide-mediated hydrogen transfer, and photoinduced electron, energy, or hydrogen atom transfer provide distinct and often complementary reactivity orders enabling predictable reductions even in complex molecules. This review discusses the main mechanisms and categorizes them based on the reducible substrate classes and the tolerance of Lewis-basic motifs, highlighting methods with particular relevance to medicinal chemistry applications.

SynthesisVol. 58(04)
University of Wuppertal (DE), Max-Planck-Institut für Kohlenforschung (DE), Ruhr University Bochum (DE)
Openalex Percentile: Top 72%
Radical Photochemical Reactions
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