Oxazoline synthesis of 1,2-trans-2-acetamido-2-deoxyglycosides. Glycosylation of secondary hydroxyl groups in partially protected saccharides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference21 articles.
1. Synthese von 6‐β‐ N ‐Acetylglucosaminido‐ d ‐glucose und ‐ d ‐galaktose
2. The Synthesis of 2-Acetamido-3-O-(D-1-carboxyethyl)-2-deoxy-α-D-glucose (N-Acetylmuramic Acid) and of Benzyl Glycoside Derivatives of 2-Amino-3-O-(D-1-carboxyethyl)-2-deoxy-D-glucose (Muramic Acid)1
3. The synthesis of a 2-amino-2-deoxy-d-glucosyl-muramic acid disaccharide: 2-acetamido-6-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-d-glucopyranosyl)-i,4-di-O-acetyl-2-deoxy- 3-O-[d-i-(methyl carboxylate)ethyl]- α-d-glucopyranose
4. Lysozyme substrates. Synthesis of p-nitrophenyl 2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2-deoxy-β-D-glucopyranoside and its β-D-(1 → 6) isomer
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