Dispiroketals in synthesis (part 7): Protection of D-glucopyranose substrates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Dispiroketals in synthesis (part 2): A new group for the selective protection of diequatorial vicinal diols in carbohydrates.
2. Dispiroketals in synthesis (Part 5): A new opportunity for oligosaccharide synthesis using differentially activated glycosyl donors and acceptors
3. Dispiroketals in Synthesis (Part 3):1Selective Protection of Diequatorial Vicinal Diols in Carbohydrates
4. Triphenylphosphine hydrobromide: A mild and efficient catalyst for tetrahydropyranylation of tertiary alcohols
5. THE MERCAPTOLYSIS OF GLUCOSE AND GALACTOSE PENTAACETATES
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1. Dispiroketals in synthesis (Part 16): Functionalised dispiroketals as new chiral auxiliaries; the synthesis of dihydroxylated dispiroketals in optically pure form and their application as bifunctional, C2-symmetrical, chiral auxiliaries for highly stereos;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. ChemInform Abstract: Dispiroketals in Synthesis. Part 7. Protection of D-Glucopyranose Substrates.;ChemInform;2010-08-19
3. A Survey of Ley’s Reactivity Tuning in Oligosaccharide Synthesis;Reactivity Tuning in Oligosaccharide Assembly;2010
4. Reactions at Oxygen Atoms;Glycoscience;2008
5. Methyl 2,3-O-(6,6′-Octahydro-6,6′-Bi-2H-Pyran-2,2′-Diyl)-α-D-Galactopyranoside;Organic Syntheses;2003-04-28
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