Doubly carbon-branched pentoses: synthesis of both enantiomers of 2,4-di-C-methyl arabinose and 2-deoxy-2,4-di-C-methyl arabinose using only acetonide protection-Reference-Cited by-同舟云学术

Doubly carbon-branched pentoses: synthesis of both enantiomers of 2,4-di-C-methyl arabinose and 2-deoxy-2,4-di-C-methyl arabinose using only acetonide protection

Published:2009-09 Issue:36 Volume:50 Page:5088-5093
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Victoria Booth K.,Jenkinson Sarah F.,Best Daniel,Nieto Fernando Fernández,Estévez Ramón J.,Wormald Mark R.,Weymouth-Wilson Alexander C.,Fleet George W.J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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1. Organisation of the Biosynthetic Gene Cluster and Tailoring Enzymes in the Biosynthesis of the Tetracyclic Quinone Glycoside Antibiotic Polyketomycin

2. The role of carbohydrates in biologically active natural products

3. Total Synthesis of Apoptolidin A

4. Total Synthesis and Structural Revision of Callipeltoside C

5. Structure of an Atypical O-Antigen Polysaccharide of Helicobacter pylori Containing a Novel Monosaccharide 3-C-Methyl-d-mannose

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