Preparation of a Protected 3-Deoxy-d-manno-oct-2-ulosonate Glycal Donor for the Synthesis of β-KDO-Containing Oligosaccharides
Author:
Affiliation:
1. Applied Chemistry Department, National Chiao Tung University, 1001 Ta Hsueh Road, Taiwan
2. Chemistry Department, National Tsing Hua University, Guang Fu Road, Taiwan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol500275j
Reference49 articles.
1. Rhizobium fredii and Rhizobium meliloti produce 3-deoxy-D-manno-2-octulosonic acid-containing polysaccharides that are structurally analogous to group II K antigens (capsular polysaccharides) found in Escherichia coli
2. Sinorhizobium meliloti strain 1021 produces a low-molecular-mass capsular polysaccharide that is a homopolymer of 3-deoxy-D-manno-oct-2-ulosonic acid harboring a phospholipid anchor
3. Chemical Structure of the Core Region of Lipopolysaccharides. An Update.
4. aCorbett, D.; Hudson, T.; Roberts, I. S.Prokaryotic Cell Wall Compounds;Konig, H.; Claus, H.; Varma, A., Eds.Springer:Heidelberg, 2010; pp111–132.
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1. 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
2. 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
3. Kdo Glycosylations and Their Application in Oligosaccharide Synthesis**;European Journal of Organic Chemistry;2023-06-05
4. α-Stereoselective 3-Deoxy-d-manno-oct-2-ulosonoic Acid (Kdo) O-Glycosylation with a p-Toluenethioglycoside Donor by the (p-Tol)2SO/Tf2O Preactivation Strategy;Organic Letters;2023-05-30
5. Hydroxamate-directed access to β-Kdo glycosides;Chemical Communications;2023
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