The synthesis of (R)- and (S)-3-(4-hydroxyphenyl)-1-methylpropyl-β-D-glucopyranosides has been achieved by two enzymatic steps, namely an oxido-reduction step involving alcohol dehydrogenases from different origin for the preparation of both aglycones in enantiomeric pure form, and a transglycosidation step involving a thermophilic β-glucosidase from the archaeon Sulfolobus solfataricus. © 1996 OPA (Overseas Publishers Association) Amsterdam B.V. Published in The Netherlands under license by Gordon and Breach Science Publishers SA.

Enzymatic routes for the synthesis of rhododendrin and epi-rhododendrin

FANTIN, Giancarlo;FOGAGNOLO, Marco
1996

Abstract

The synthesis of (R)- and (S)-3-(4-hydroxyphenyl)-1-methylpropyl-β-D-glucopyranosides has been achieved by two enzymatic steps, namely an oxido-reduction step involving alcohol dehydrogenases from different origin for the preparation of both aglycones in enantiomeric pure form, and a transglycosidation step involving a thermophilic β-glucosidase from the archaeon Sulfolobus solfataricus. © 1996 OPA (Overseas Publishers Association) Amsterdam B.V. Published in The Netherlands under license by Gordon and Breach Science Publishers SA.
1996
Trincone, ; E., Pagnotta; Fantin, Giancarlo; Fogagnolo, Marco
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1202080
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