Issue 31, 2025

Direct organocatalytic esterification of carboxylic acids and alcohols by redox neutral sulfur(iv) catalysis via intramolecularly interrupted Pummerrer intermediates

Abstract

Design, synthesis, and catalytic activity of new sulfur(IV) based organocatalysts for the direct esterification of carboxylic acids and alcohols is unveiled. The polar nature of the sulfoxide in the phenol-tethered catalyst accelerates the formation of an intramolecularly interrupted Pummerrer intermediate that further facilitates the catalytic esterification reaction via the activation of carboxylic acids.

Graphical abstract: Direct organocatalytic esterification of carboxylic acids and alcohols by redox neutral sulfur(iv) catalysis via intramolecularly interrupted Pummerrer intermediates

Supplementary files

Article information

Article type
Communication
Submitted
30 Jan 2025
Accepted
16 Mar 2025
First published
17 Mar 2025
This article is Open Access
Creative Commons BY license

Chem. Commun., 2025,61, 5746-5749

Direct organocatalytic esterification of carboxylic acids and alcohols by redox neutral sulfur(IV) catalysis via intramolecularly interrupted Pummerrer intermediates

A. Biswas, P. Pradhan, S. A. Wakpanjar and P. K. Kancharla, Chem. Commun., 2025, 61, 5746 DOI: 10.1039/D5CC00556F

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