Show legend Show as text

Structure type: fragment of a bigger structure
Aglycon: (2->6)lipid A
Trivial name: Kdo-antigen of Chlamydiaceae
Compound class: core oligosaccharide
Contained glycoepitopes: IEDB_130650,IEDB_130657,IEDB_130658,IEDB_130659

• Article ID: 4973
  Kosma P "Progress in Kdo-glycoside chemistry" - Tetrahedron Letters 57(20) (2016) 2133-2142
  

  Glycosylation chemistry of 3-deoxy-D-manno-oct-2-ulosonic acid units has been considerably developed within the last decade. This review covers major achievements with respect to improved yields and anomeric selectivity as well as suppression of the elimination side reaction via selection of dedicated protecting groups and appropriate activation of the anomeric center.

  synthesis, oligosaccharide, 3-deoxy-D-manno-oct-2-ulosonic acid, Kdo, glycosyl donor, Glycal

  Publication DOI: 10.1016/j.tetlet.2016.04.005
  Journal NLM ID: 2984819R
  Publisher: Elsevier
  Correspondence: paul.kosma@boku.ac.at
  Institutions: University of Natural Resources and Life Sciences-Vienna, Department of Chemistry, Muthgasse 18, A-1190 Vienna, Austria
  
   
  
  (Chlamydiaceae)
  CSDB ID 11849 (all data & tools)

Show legend Show as text

Structure type: fragment of a bigger structure
Aglycon: (2->6)lipid A
Trivial name: Kdo-antigen of Chlamydiaceae
Compound class: core oligosaccharide
Contained glycoepitopes: IEDB_130650,IEDB_130659,IEDB_150901

• Article ID: 4973
  Kosma P "Progress in Kdo-glycoside chemistry" - Tetrahedron Letters 57(20) (2016) 2133-2142
  

  Glycosylation chemistry of 3-deoxy-D-manno-oct-2-ulosonic acid units has been considerably developed within the last decade. This review covers major achievements with respect to improved yields and anomeric selectivity as well as suppression of the elimination side reaction via selection of dedicated protecting groups and appropriate activation of the anomeric center.

  synthesis, oligosaccharide, 3-deoxy-D-manno-oct-2-ulosonic acid, Kdo, glycosyl donor, Glycal

  Publication DOI: 10.1016/j.tetlet.2016.04.005
  Journal NLM ID: 2984819R
  Publisher: Elsevier
  Correspondence: paul.kosma@boku.ac.at
  Institutions: University of Natural Resources and Life Sciences-Vienna, Department of Chemistry, Muthgasse 18, A-1190 Vienna, Austria
  
   
  
  (Chlamydiaceae)
  CSDB ID 11850 (all data & tools)

Show legend Show as text

Structure type: fragment of a bigger structure
Aglycon: (2->6)lipid A
Trivial name: Kdo-antigen of Chlamydiaceae
Compound class: core oligosaccharide
Contained glycoepitopes: IEDB_130650,IEDB_130657,IEDB_130658,IEDB_130659,IEDB_150756,IEDB_150901,IEDB_151769

• Article ID: 4973
  Kosma P "Progress in Kdo-glycoside chemistry" - Tetrahedron Letters 57(20) (2016) 2133-2142
  

  Glycosylation chemistry of 3-deoxy-D-manno-oct-2-ulosonic acid units has been considerably developed within the last decade. This review covers major achievements with respect to improved yields and anomeric selectivity as well as suppression of the elimination side reaction via selection of dedicated protecting groups and appropriate activation of the anomeric center.

  synthesis, oligosaccharide, 3-deoxy-D-manno-oct-2-ulosonic acid, Kdo, glycosyl donor, Glycal

  Publication DOI: 10.1016/j.tetlet.2016.04.005
  Journal NLM ID: 2984819R
  Publisher: Elsevier
  Correspondence: paul.kosma@boku.ac.at
  Institutions: University of Natural Resources and Life Sciences-Vienna, Department of Chemistry, Muthgasse 18, A-1190 Vienna, Austria
  
   
  
  (Chlamydiaceae)
  CSDB ID 11851 (all data & tools)