Carbohydrates as nucleophiles in conjugate addition for preparation of muramic acid analogues
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference28 articles.
1. Hexosamine-containing peptides in spores of Bacillus subtilis, B. megatherium and B. cereus
2. The isolation, characterization and chemical synthesis of muramic acid
3. Stereospecific Synthesis of 2-Amino-3-O-(D-1'-carboxyethyl)-2-deoxy-D-glucose (Muramic Acid) and Related Compounds1,2
4. Minimal structural requirements for adjuvant activity of bacterial peptidoglycan derivatives
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1. ChemInform Abstract: Carbohydrates as Nucleophiles in Conjugate Addition for Preparation of Muramic Acid Analogues.;ChemInform;2010-08-17
2. Multiple and Regioselective Introduction of Protected Sulfates into Carbohydrates Using Sulfuryl Imidazolium Salts;The Journal of Organic Chemistry;2009-11-19
3. Chemoenzymatic synthesis of Park’s nucleotide: toward the development of high-throughput screening for MraY inhibitors;Tetrahedron Letters;2007-01
4. Synthesis of Linear and Branched Regioisomeric Chitooligosaccharides as Potential Mimetics of Natural Oligosaccharide Ligands of Natural Killer Cells NKR-P1 and CD69 Lectin Receptors;Collection of Czechoslovak Chemical Communications;2004
5. Synthesis and biological evaluation of new UDP-GalNAc analogues for the study of polypeptide-α-GalNAc-transferases;Bioorganic & Medicinal Chemistry Letters;2003-06
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