1,6-Anhydro-2,3-O-(4-methoxybenzylidene)-β-D-mannopyranose: A useful synthon for the preparation of valuable disaccharides
Author:
Publisher
Wiley
Subject
General Chemistry
Reference12 articles.
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2. A facile formation of 2,5-anhydro sugars by ring contraction in methyl hexopyranoside 2-triflates under conditions of nucleophilic displacement;Carbohydrate Research;1989-04
3. Benzyl-2,4-Diacetamido-2, 4,6-Tri-Deoxy-α(β) -D-Galactopyranoside;Journal of Carbohydrate Chemistry;1987-09
4. Synthesis of 1,6-Anhydro-2-O-trifluoromethanesulphonyl-0-D-mannopyranose Derivatives and Their Conversion Into the Corresponding 1.6-Anhydro-2-azido-2-deoxy-β-D-glucopyranoses: A Convenient and Efficient Approach;Journal of Carbohydrate Chemistry;1986-06
5. Alternative synthesis and regioselective coupling of 1,6-anhydro-2-azido- and -2-phthalimido-2-deoxy-β-D-galactopyranose;Recueil des Travaux Chimiques des Pays-Bas;1986
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