Glycosylation Chemistry of 3-Deoxy-D-manno-Oct-2-ulosonic Acid (Kdo) Donors
Author:
Publisher
Wiley
Subject
General Chemistry
Reference111 articles.
1. Chemical Diversity in the Sialic Acids and Related α-Keto Acids: An Evolutionary Perspective
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1. Stereoselective synthesis of α-3-deoxy-ᴅ-manno-oct-2-ulosonic acid (α-Kdo) derivatives using a C3-p-tolylthio-substituted Kdo fluoride donor;Chinese Chemical Letters;2024-05
2. Additive-assisted synthesis of α-Kdo glycosides with peracetylated glycosyl ynenoate as a donor;Organic & Biomolecular Chemistry;2024
3. Stereocontrolled Synthesis of α‐3‐Deoxy‐d‐manno‐oct‐2‐ulosonic Acid (α‐Kdo) Glycosides Using C3‐p‐Tolylthio‐Substituted Kdo Donors: Access to Highly Branched Kdo Oligosaccharides;Angewandte Chemie International Edition;2023-12-08
4. Stereocontrolled Synthesis of α‐3‐Deoxy‐d‐manno‐oct‐2‐ulosonic Acid (α‐Kdo) Glycosides Using C3‐p‐Tolylthio‐Substituted Kdo Donors: Access to Highly Branched Kdo Oligosaccharides;Angewandte Chemie;2023-12-08
5. Kdo Glycosylations and Their Application in Oligosaccharide Synthesis**;European Journal of Organic Chemistry;2023-06-05
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