Regioselective enzymatic hydrolysis of acetylated pyranoses and pyranosides using immobilised lipases. An easy chemoenzymatic synthesis of α- and β-d-glucopyranose acetates bearing a free secondary C-4 hydroxyl group-Reference-Cited by-同舟云学术

Regioselective enzymatic hydrolysis of acetylated pyranoses and pyranosides using immobilised lipases. An easy chemoenzymatic synthesis of α- and β-d-glucopyranose acetates bearing a free secondary C-4 hydroxyl group

Published:2002-10 Issue:18 Volume:337 Page:1615-1621
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Terreni Marco,Salvetti Raul,Linati Laura,Fernandez-Lafuente Roberto,Fernández-Lorente Gloria,Bastida Agatha,Guisan José M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference14 articles.

1. The Stereoselective Dehydrative α-Glucosylation Using 6-O-Acetyl- and 6-O-p-Nitrobenzoyl-2,3,4-tri-O-benzyl-D-glucopyranoses

2. Glucosidation of Tetra-O-benzyl-α-D-glucose with Chlorosilane and Silver Sulfonate

3. Synthesis of glycosyl halides and glycosides via 1-O-sulfonyl derivatives

4. Lipase-Catalyzed Regioselective Acylation and Deacylation of Glucose Derivatives

5. A practical synthesis of 1,2.3.6-tetra-O-acetyl-α- and β-D-glucopyranose, and their use to prepare trisaccharides

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