Issue 6, 2026

Multi-step biocatalytic strategy to produce a library of original xylosides with various ester functions for cosmetic applications

Abstract

A biocatalytic strategy was developed to prepare a series of β-xylopyranosides with one or two ester functions using a multistep enzymatic transformation from biobased xylans. Transglycosylation reactions with α,ω-diols were first performed using a commercially available xylanase to produce β-xylosides in good yields. In a second step, a selective esterification of the primary hydroxyl group of the aglycone moiety was carried out by reaction with carboxylic acids of cosmetic interest catalyzed by an immobilized commercial lipase. Finally a transesterification step led to the formation of xylosides esterified with two different acyl chains.

Graphical abstract: Multi-step biocatalytic strategy to produce a library of original xylosides with various ester functions for cosmetic applications

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Article information

Article type
Paper
Submitted
08 Dec 2025
Accepted
16 Jan 2026
First published
26 Jan 2026
This article is Open Access
Creative Commons BY license

RSC Adv., 2026,16, 5632-5639

Multi-step biocatalytic strategy to produce a library of original xylosides with various ester functions for cosmetic applications

E. Jolly, M. Muzard, R. Plantier-Royon and C. Rémond, RSC Adv., 2026, 16, 5632 DOI: 10.1039/D5RA09500J

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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