Synthesis and glycosidic coupling reaction of substituted 2,6-dioxabicyclo[3.1.0]hexanes: 1,2-anhydro-3,5-di-O-benzyl-α-d-ribofuranose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference30 articles.
1. Strategies for antiviral therapy in AIDS
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1. ChemInform Abstract: Synthesis and Glycosidic Coupling Reaction of Substituted 2,6- Dioxabicyclo(3.1.0)hexanes: 1,2-Anhydro-3,5-di-O-benzyl-α-D- ribofuranose.;ChemInform;2010-08-03
2. Synthesis and biochemical evaluation of O-acetyl-ADP-ribose and N-acetyl analogs;Organic & Biomolecular Chemistry;2007
3. Alkylalanes and methyl furanosides: regioselective O-debenzylation or acetal cleavage;Carbohydrate Research;2006-09
4. Oxetane δ‐Amino Acids: Chemoenzymatic Synthesis of 2,4‐Anhydro‐5‐N‐(t‐butoxycarbonyl)amino‐D‐lyxonic Acid;Journal of Carbohydrate Chemistry;2006-05-01
5. 1,2-Anhydrosaccharides and 1,2-Cyclic Sulfites as Saccharide Donors in Convergent Synthesis of Glucopyranosyl-, Mannopyranosyl- and Ribofuranosylbenzocamalexin;Collection of Czechoslovak Chemical Communications;2005
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