Iterative One-Carbon Homologation of Unmodified Carboxylic Acids

The one-carbon homologation of carboxylic acids is a valuable route to construct families of homologues, which play fundamental roles in chemistry and biology. However, known procedures are based on multistep sequences, use harsh conditions or are limited in scope. Thus, almost a century after the discovery of the original Arndt-Eistert homologation sequence, a general method to directly convert carboxylic acids into their corresponding homologues remains elusive. Exploiting the photoredox reactivity of nitroethylene, we disclose a practical visible-light-induced homologation of unmodified carboxylic acids. Iterations of the procedure reveal an exceptionally tunable strategy for the construction of inert carbon spacers, opening new opportunities in synthesis.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-12-10
DOI
https://doi.org/10.1021/jacs.4c13630
Citations
22
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
5.50

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article

Iterative One-Carbon Homologation of Unmodified Carboxylic Acids

Mattia Silvi, Heorhii Melnychenko, Emilie Wheatley
22 citations
Journal of the American Chemical Society
Radical Photochemical Reactions
5.50
article

Iterative One-Carbon Homologation of Unmodified Carboxylic Acids

Mattia Silvi, Heorhii Melnychenko, Emilie Wheatley
article en
22 citations

Abstract

The one-carbon homologation of carboxylic acids is a valuable route to construct families of homologues, which play fundamental roles in chemistry and biology. However, known procedures are based on multistep sequences, use harsh conditions or are limited in scope. Thus, almost a century after the discovery of the original Arndt-Eistert homologation sequence, a general method to directly convert carboxylic acids into their corresponding homologues remains elusive. Exploiting the photoredox reactivity of nitroethylene, we disclose a practical visible-light-induced homologation of unmodified carboxylic acids. Iterations of the procedure reveal an exceptionally tunable strategy for the construction of inert carbon spacers, opening new opportunities in synthesis.

Journal of the American Chemical SocietyVol. 146(50)
University of Nottingham (GB)
UK Research and Innovation, University of Nottingham, HORIZON EUROPE Framework Programme, Engineering and Physical Sciences Research Council, School of Chemistry, University of Nottingham
Openalex Percentile: Top 3%
Radical Photochemical Reactions
5.50
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