Development of Mild Palladium‐Catalyzed N‐Arylation of Ortho‐Acylanilines in Rhamnolipid Micellar System

BuXPhos system enables high yields at 40°C, significantly lower than conventional methods (>100°C), with broad substrate scope. This industrially produced biodegradable surfactant system offers a sustainable alternative to organic solvents, combining enhanced reactivity with improved energy efficiency and environmental compatibility.

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Publication Details

Journal
ChemSusChem
Published
2026-04-12
DOI
https://doi.org/10.1002/cssc.70609
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Development of Mild Palladium‐Catalyzed N‐Arylation of Ortho‐Acylanilines in Rhamnolipid Micellar System

Zoltán Novàk, Johannes Lehmann, Péter R. Kollár, Attila R. Herczegh
ChemSusChem
Catalytic Cross-Coupling Reactions
article

Development of Mild Palladium‐Catalyzed N‐Arylation of Ortho‐Acylanilines in Rhamnolipid Micellar System

Zoltán Novàk, Johannes Lehmann, Péter R. Kollár, Attila R. Herczegh
article en

Abstract

BuXPhos system enables high yields at 40°C, significantly lower than conventional methods (>100°C), with broad substrate scope. This industrially produced biodegradable surfactant system offers a sustainable alternative to organic solvents, combining enhanced reactivity with improved energy efficiency and environmental compatibility.

ChemSusChemVol. 19(7)
Eötvös Loránd University (HU), Evonik (Germany) (DE)
Magyar Tudományos Akadémia, Nemzeti Kutatási Fejlesztési és Innovációs Hivatal, Servier, National Research, Development and Innovation Office, Evonik Operations
Affordable and clean energy
Openalex Percentile: Top 19%
Catalytic Cross-Coupling Reactions
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