Convenient preparation of α- and β-glycosides of novel isomeric 3-deoxy-hept-2-ulosaric acids diesters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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3. Identification of 2-keto-3-deoxy-1,7-dicarboxyheptonic acid as a constituent of the lipopolysaccharide of Acinetobacter calcoaceticus NCTC 10305
4. Identification of 3-deoxy-lyxo-2-heptulosaric acid in the core region of lipopolysaccharides from Rhizobiaceae
5. Partial Structure of Lipopolysaccharides Isolated from Rhizobium leguminosarum bv.trifolii 24 and Its GalA-Negative Exo− Mutant AR20
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1. ChemInform Abstract: Convenient Preparation of α- and β-Glycosides of Novel Isomeric 3-Deoxy-hept-2-ulosaric Acids Diesters.;ChemInform;2010-08-02
2. Recent Advances in the Chemistry of Bioactive 3-Deoxy-Ulosonic Acids;Bioactive Natural Products (Part K);2005
3. Synthesis of 2-deoxy-α-DAH based on diazo chemistry by insertion reactions of 2-diazo-3-deoxy- d - arabino -heptulosonate derivatives mediated by rhodium(II);Tetrahedron;2001-12
4. Observations on the oxirane ring opening reactions of a 2-acetamido-3,4-anhydro sugar and on the inversion of the derived alcohols;Tetrahedron: Asymmetry;2000-12
5. Synthesis of 3-Deoxy-α-d-manno-oct-2-ulosonic Acid Glycoside (Kdo) and Its 2-Deoxy Analogue: A Horner−Emmons Approach;Organic Letters;1999-11-02
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