The use of 2,6-anhydro-2-thio glycopyranosyl fluoride for a highly α-stereoselective glycosylation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. The use of 2,6-anhydro-2-thio sugar for a highly stereocontrolled glycosylation: A novel strategy for synthesis of 2,6-dideoxy-α-glycosides
2. The use of 2,6-anhydro-2-thio sugar for a highly stereocontrolled glycosylation: A novel strategy for synthesis of 2,6-dideoxy-α-glycosides
3. AN EFFICIENT METHOD FOR GLUCOSYLATION OF HYDROXY COMPOUNDS USING GLUCOPYRANOSYL FLUORIDE
4. Stereospecific 1,2-migrations in carbohydrates. Stereocontrolled synthesis of .alpha.- and .beta.-2-deoxyglycosides
5. Glycosylation using glucopyranosyl fluorides and silicon-based catalysts. Solvent dependency of the stereoselection
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1. Stereoselective Formation of 2-Deoxyglycosidic Bonds in Biologically Active Natural Products;Stereoselective Synthesis of Drugs and Natural Products;2013-10-02
2. Glycosyl donors in “unusual” conformations – influence on reactivity and selectivity;Comptes Rendus Chimie;2011-01
3. ChemInform Abstract: The Use of 2,6-Anhydro-2-thio Glycopyranosyl Fluoride (I) for a Highly α-Stereoselective Glycosylation.;ChemInform;2010-08-22
4. O-Glycosidation Methods;Comprehensive Glycoscience;2007
5. Novel glycosylation methods and their application to natural products synthesis;Carbohydrate Research;2006-07
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