A general, convenient synthesis of the repeating, disaccharide—dipeptide unit of the bacterial, cell-wall peptidoglycan by the oxazoline method
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference24 articles.
1. M. Kiso, Y. Kaneda, Y. Goh, A. Hasegawa, and I. Azuma, Agric. Biol. Chem., submitted for publication.
2. Minimal structural requirements for adjuvant activity of bacterial peptidoglycan derivatives
3. Total synthesis and adjuvant activity of bacterial peptidoglycan derivatives
4. Higher Immunoadjuvant Activities ofN-Acetyl-β-D-glucosaminyl-(1-4)-N-acetylmuramyl-L-alanyl-D-isoglutamine in Comparison withN-Acetylmuramyl-L-alanyl-D-isoglutamine
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1. Concise and Efficient Synthesis of 2-Acetamido-2-deoxy-β-d-hexopyranosides of Diverse Aminosugars from 2-Acetamido-2-deoxy-β-d-glucose;The Journal of Organic Chemistry;2008-12-08
2. Synthesis of an Orthogonally Protected Precursor to the Glycan Repeating Unit of the Bacterial Cell Wall;Organic Letters;2001-10-10
3. Systematic Synthesis and Molecular analysis of the Biologically Functional Glycoconjugates, and Application as Indispensable Probes for the Life Sciences;Nippon Nōgeikagaku Kaishi;1995
4. Synthesis of oligosaccharides of 2-amino-2-deoxy sugars;Chemical Reviews;1992-09
5. Convenient syntheses of O-(2-acetamido-2-deoxy-β-d-glucopyranosyl)-(1→6 and 4)-N-acetylmuramoyl-l-alanyl-d-isoglutamine;Carbohydrate Research;1989-02
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