Enzymatic synthesis of alkyl arabinofuranosides using a thermostable α-L-arabinofuranosidase

DOI: 10.1016/S0040-4039(02)02381-X

Source and publish data:

Tetrahedron Letters p. 9653 - 9655 (2002)

Update date:2022-08-04

Topics:

Authors:

Rémond, Caroline

Ferchichi, Mounir

Aubry, Nathalie

Plantier-Royon, Richard

Portella, Charles

O'Donohue, Michael J.

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Article abstract of DOI:10.1016/S0040-4039(02)02381-X

A thermostable α-L-arabinofuranosidase was tested for its ability to perform transglycosylation with different alcohol acceptors. Reactions were characterized by high rates with optimal synthesis being obtained within 10 min. Both primary and secondary al

Full text of DOI:10.1016/S0040-4039(02)02381-X

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Product name:methyl 2,3,5-tri-O-benzoyl-1-α-L-arabinofuranoside

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