Reagent for the Chemoselective Reduction of Carboxylic Acids to Aldehydes

We report the development of a multifunctional reagent for the direct conversion of carboxylic acids to aldehydes under mild conditions and with exquisite chemoselectivity. These reactions proceed in aqueous solvent at room temperature in 20 min, can be done open to air, require no metal catalysts, and employ near-stoichiometric amounts of both reducing agent and a mild base. No over-reduction, epimerization, or reduction of other reducible functional groups is observed. With this reagent, a broad scope of complex, drug-like aryl and alkyl carboxylic acids can be reduced directly to aldehydes.

Authors

Institutions

Publication Details

Journal
Organic Letters
Published
2025-10-23
DOI
https://doi.org/10.1021/acs.orglett.5c04063
Citations
3
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
1.61
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Reagent for the Chemoselective Reduction of Carboxylic Acids to Aldehydes

Patrick S. Fier, Ethan Fung, Kevin M. Maloney
3 citations
Organic Letters
Asymmetric Hydrogenation and Catalysis
1.61
article

Reagent for the Chemoselective Reduction of Carboxylic Acids to Aldehydes

Patrick S. Fier, Ethan Fung, Kevin M. Maloney
article en
3 citations

Abstract

We report the development of a multifunctional reagent for the direct conversion of carboxylic acids to aldehydes under mild conditions and with exquisite chemoselectivity. These reactions proceed in aqueous solvent at room temperature in 20 min, can be done open to air, require no metal catalysts, and employ near-stoichiometric amounts of both reducing agent and a mild base. No over-reduction, epimerization, or reduction of other reducible functional groups is observed. With this reagent, a broad scope of complex, drug-like aryl and alkyl carboxylic acids can be reduced directly to aldehydes.

Organic LettersVol. 27(44)
Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
Openalex Percentile: Top 15%
Asymmetric Hydrogenation and Catalysis
1.61
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.