Chemo-enzymatic synthesis of an original arabinofuranosyl cluster: Optimization of the enzymatic conditions

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Abstract

The evaluation of a mutated glycosidase as a major, renewable and eco-friendly partner of the glycosylation reaction allowed the one step synthesis of the arabinofuranosyl cluster 4 in 38% yield. Our mutated biocatalyst was able to perform coupling to a multivalent bulky substituent with 80% yield on each arm and pave the way for the further development of enzymatic means of ligation of carbohydrates onto organic scaffolds. ©ARKAT-USA, Inc.

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Almendros, M., François-Heude, M., Legentil, L., Nugier-Chauvin, C., Daniellou, R., & Ferrières, V. (2012). Chemo-enzymatic synthesis of an original arabinofuranosyl cluster: Optimization of the enzymatic conditions. Arkivoc, 2013(2), 123–132. https://doi.org/10.3998/ark.5550190.0014.211

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