ArticleRSC advances2026
Multi-step biocatalytic strategy to produce a library of original xylosides with various ester functions for cosmetic applications.
Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
4 authors.
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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.
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Registered trials
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