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ChemInform Abstract: Diastereoselective Hydrogenations of α-(2′,3′,4′,6′-Tetra-O- acetyl-β-D-glucopyranosyloxymethylene) Carboxylic Esters: A Route to Stereopure Aldol Derivatives.

✍ Scribed by D. S. LARSEN; A. SCHOFIELD; R. J. STOODLEY; P. D. TIFFIN

Book ID: 112021477
Publisher: John Wiley and Sons
Year: 2010
Weight: 36 KB
Volume: 26
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199518037

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ChemInform Abstract: Regio- and Stereoselective Bromo(alkoxylation)s of (E)-α- (2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyloxymethylene) Carbonyl Compounds. A Route to Near-Stereopure α-Bromo α-Dioxymethyl Carbonyl Compounds.

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ChemInform Abstract: Stereoselective Epoxidations of Vinylogous Esters/Carbonates Directed by the 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Auxiliary: A Route to Near Stereopure Tertiary Alcohols Bearing Functional Arms.

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ChemInform Abstract: A Highly Diastereoselective, Practical Synthesis of Allyl, Propargyl 2,3,4,6-Tetra-O-acetyl-β-D-gluco, β-D-Galactopyranosides and Allyl, Propargyl Heptaacetyl-β-D-lactosides.

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