Carbohydrates as chiral auxiliaries: synthesis of 2-hydroxy-β-D-glucopyranosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Carbohydrates as chiral auxiliaries: asymmetric cyclopropanation reaction of acyclic olefins
2. On the direct epoxidation of glycals: application of a reiterative strategy for the synthesis of .beta.-linked oligosaccharides
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4. Oxidations by methyl(trifluoromethyl)dioxirane. 2. Oxyfunctionalization of saturated hydrocarbons
5. The use of 2-O-acyl-1-O-sulfonyl-d-galactopyranose derivatives in β-d-galactopyranoside synthesis
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1. “One-pot” access to α-d-mannopyranosides from glycals employing ruthenium catalysis;RSC Adv.;2014
2. Sequential Directed Epoxydation-Acidolysis from Glycals with MCPBA. A Flexible Approach to Protected Glycosyl Donors;The Journal of Organic Chemistry;2011-11-08
3. Stereoselective Tandem Epoxidation-Alcoholysis/Hydrolysis of Glycals with Molybdenum Catalysts;Advanced Synthesis & Catalysis;2010-12-07
4. ChemInform Abstract: Carbohydrates as Chiral Auxiliaries: Synthesis of 2-Hydroxy-β-D- glucopyranosides.;ChemInform;2010-08-21
5. Tandem Epoxidation‐Alcoholysis or Epoxidation‐Hydrolysis of Glycals Catalyzed by Titanium(IV) Isopropoxide or Venturello’s Phosphotungstate Complex;Advanced Synthesis & Catalysis;2008-07-07
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