Catalytic Amidation of Carboxylic Acids Using <i>ortho</i> -Aminophenylboronic Acids

ortho-Substituted boronic acids have demonstrated significant potential as catalysts for direct amidation reactions, providing a sustainable alternative to conventional coupling reagents. We report the screening of ortho-functionalized arylboronic acids, including four literature benchmarks, as catalysts for the direct condensation of amines and carboxylic acids. The commercially available ortho-aminophenylboronic acids, specifically (2-(piperidin-1-yl)phenyl)boronic acid (2-PPBA), emerge as the optimal catalyst, providing amides from a range of carboxylic acids and amines.

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Publication Details

Journal
ACS Organic & Inorganic Au
Published
2026-05-12
DOI
https://doi.org/10.1021/acsorginorgau.6c00021
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Catalytic Amidation of Carboxylic Acids Using ortho -Aminophenylboronic Acids

Mikko Passiniemi, Petri M. Pihko, Veera K. Bruce-Salmenkivi
ACS Organic & Inorganic Au
Chemical Synthesis and Analysis
article

Catalytic Amidation of Carboxylic Acids Using ortho -Aminophenylboronic Acids

Mikko Passiniemi, Petri M. Pihko, Veera K. Bruce-Salmenkivi
article en

Abstract

ortho-Substituted boronic acids have demonstrated significant potential as catalysts for direct amidation reactions, providing a sustainable alternative to conventional coupling reagents. We report the screening of ortho-functionalized arylboronic acids, including four literature benchmarks, as catalysts for the direct condensation of amines and carboxylic acids. The commercially available ortho-aminophenylboronic acids, specifically (2-(piperidin-1-yl)phenyl)boronic acid (2-PPBA), emerge as the optimal catalyst, providing amides from a range of carboxylic acids and amines.

ACS Organic & Inorganic Au
Orion Corporation (Finland) (FI), University of Jyväskylä (FI)
Orion Corporation
Openalex Percentile: Top 8%
Chemical Synthesis and Analysis
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