Chemo-, stereo- and regioselective hydrogenolysis of carbohydrate benzylidene acetals. Synthesis of benzyl ethers of benzyl α-d-, methyl β-D-mannopyranosides and benzyl α-D-rhamnopyranoside by ring cleavage of benzylidene derivatives with the LiAlH4-AlCl3 reagent
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Synthesis of O-β-D-galactopyranosyl-(1→4)-O-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→3)-D-mannose, a postulated trisaccharide of human erythrocyte membrane sialoglycoprotein
2. Synthesis of β--mannopyranosides and regioselective -alkylation of dibutylstannylene complexes
3. Synthesis of 3,6-Di-O-(alpha-D-mannopyranosyl)-D-mannose.
4. Regioselective enhancement of the nucleophilicity of hydroxyl groups through trialkylstannylation: a route to partial alkylation of polyhydroxy compounds
5. Synthesis of hepta- and penta-saccharides, part of the complex-type carbohydrate portion of glycoproteins
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