Synthesis of Anemoclemoside B, the First Natural Product with an Open-Chain Cyclic Acetal Glycosidic Linkage
- 21 April 2005
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 7 (10) , 1935-1938
- https://doi.org/10.1021/ol050324y
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Structural analysis of the lipopolysaccharide derived core oligosaccharides of Actinobacillus pleuropneumoniae serotypes 1, 2, 5a and the genome strain 5bCarbohydrate Research, 2004
- Characterisation of a tetrasaccharide released on mild acid hydrolysis of LPS from two rough strains of Shewanella species representing different DNA homology groupsCarbohydrate Research, 2004
- The structure of the rough-type lipopolysaccharide from Shewanella oneidensis MR-1, containing 8-amino-8-deoxy-Kdo and an open-chain form of 2-acetamido-2-deoxy-d-galactoseCarbohydrate Research, 2003
- The structure of the carbohydrate backbone of the core–lipid A region of the lipopolysaccharide from Proteus penneri strain 40: new Proteus strains containing open-chain acetal-linked N-acetylgalactosamine in the core part of the LPSCarbohydrate Research, 2001
- The structure of the core part of Proteus vulgaris OX2 lipopolysaccharideCarbohydrate Research, 1999
- Sugars out in the openNature, 1999
- The structure of the core part of Proteus mirabilis O27 lipopolysaccharide with a new type of glycosidic linkageCarbohydrate Research, 1999
- A New Type of Glycosidic Linkage: An Open-Chain Acetal-LinkedN-Acetylgalactosamine in the Core Part of the Lipopolysaccharides fromProteus MicroorganismsAngewandte Chemie International Edition in English, 1999
- Triterpenoid glycosides from Anemoclema glaucifoliumPhytochemistry, 1995
- Synthesis, Conformational Analysis, and the Glycosidic Coupling Reaction of Substituted 2,7-Dioxabicyclo[4.1.0]Heptanes: 1,2-Anhydro-3,4-di-O-Benzyl-β-L-arabinopyranoseJournal of Carbohydrate Chemistry, 1994