A novel, reductive ring-opening of carbohydrate benzylidene acetals, with unusual regioselectivity
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference11 articles.
1. Synthesis of 4-O-α-d-galactopyranosyl-l-rhamnose and 4-O-α-d-galactopyranosyl-2-O-β-glucopyranosyl-l-rhamnose using dioxolane-type benzylidene acetals as temporary protecting-groups
2. Stereoselective ring-cleavage of 3-O-benzyl- and 2,3-di-O-benzyl-4,6-O-benzylidenehexopyranoside derivatives with the LiAlH4AlCl3, reagent
3. An efficient reduction of acetals and ketals to methyl ethers.
4. Novel reagent system for converting a hydroxy-group into an iodo-group in carbohydrates with inversion of configuration. Part 2
5. Rapid chromatographic technique for preparative separations with moderate resolution
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1. Stereodirecting Effect of Esters at the 4-Position of Galacto- and Glucopyranosyl Donors: Effect of 4-C-Methylation on Side-Chain Conformation and Donor Reactivity, and Influence of Concentration and Stoichiometry on Distal Group Participation;The Journal of Organic Chemistry;2023-09-07
2. Regioselective Reductive Opening of Benzylidene Acetals with Dichlorophenylborane/Triethylsilane: Previously Unreported Side Reactions and How to Prevent Them;The Journal of Organic Chemistry;2022-01-11
3. Systematic Study of Regioselective Reductive Ring-Opening Reactions of 4,6-O-Halobenzylidene Acetals of Glucopyranosides;The Journal of Organic Chemistry;2021-09-03
4. Synthesis of Carbohydrate Building Blocks for Automated Oligosaccharide Construction;Comprehensive Glycoscience;2021
5. Protecting Group Manipulations in Carbohydrate Synthesis;Comprehensive Glycoscience;2021
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