Methyl 6-O-butyryl-alpha-D- and L-glucopyranosides and methyl 6-deoxy-alpha-D- and L-glucopyranosides have been submitted to lipase catalyzed butyrylation, using porcine pancreatic, Candida cylindracea, and Pseudomonas cepacia lipases in organic solvents. The influence of the orientation of the secondary hydroxyl groups on the regioselectivity of the butyrylation is discussed.

Enzymic Acylation of Methyl D-glucopyranosides and L-glucopyranosides and 6-deoxy-glucopyranosides

TOMA, LUCIO
1992-01-01

Abstract

Methyl 6-O-butyryl-alpha-D- and L-glucopyranosides and methyl 6-deoxy-alpha-D- and L-glucopyranosides have been submitted to lipase catalyzed butyrylation, using porcine pancreatic, Candida cylindracea, and Pseudomonas cepacia lipases in organic solvents. The influence of the orientation of the secondary hydroxyl groups on the regioselectivity of the butyrylation is discussed.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/453830
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