The selective benzoylation of methyl 4,6-O-benzylidene-α-d-glycopyranosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference13 articles.
1. Monotosylation of diols using phase-transfer catalysis
2. Synthesis of partially protected benzyl and methyl α-l-rhamnopyranosides by the phase-transfer technique
3. Synthesis of Sulfonic Esters under Phase-Transfer Catalysed Conditions
4. The Phase-Transfer Catalysed Synthesis of Esters of Carboxylic Acids
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1. Regioselective Protection at the Secondary Positions of Carbohydrates with Acyclic Protecting Groups;Protecting Groups;2018-11-19
2. Glycosyl nitrates in synthesis: streamlined access to glucopyranose building blocks differentiated at C-2;Organic & Biomolecular Chemistry;2018
3. Regioselective Benzoylation of 4,6-O-Benzylidene Acetals of Glycopyranosides in the Presence of Transition Metals;Journal of Carbohydrate Chemistry;2015-01-02
4. Relative Reactivity of Hydroxyl Groups in Monosaccharides;Carbohydrates;2009-08-03
5. Synthesis and Partial Biological Evaluation of a Small Library of Differentially-Linked β-C-Disaccharides1;The Journal of Organic Chemistry;2003-05-14
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