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Structure type: polymer chemical repeating unit ; n=1900
Trivial name: acidic polysaccharide
Contained glycoepitopes: IEDB_135813,IEDB_137340,IEDB_141807,IEDB_151531

• Article ID: 1541
  Litjens RE, den Heeten R, Timmer MS, Overkleeft HS, van der Marel GA "An expedient synthesis of the repeating unit of the acidic polysaccharide of the bacteriolytic complex of lysoamidase" - Chemistry 11(3) (2005) 1010-1016
  

  The first synthesis of the trisaccharide repeating unit of the acidic polysaccharide of the bacteriolytic complex of lysoamidase is presented. The construction is based on a linear glycosylation strategy that starts from the reducing end and employs thio- and selenoglycosides in a highly stereoselective manner by a single set of activation conditions. The thus-formed trisaccharide is selectively deprotected and oxidised, after which a final deprotection step furnishes the desired repeating unit

  synthesis, chemistry, polysaccharide, repeating unit, trisaccharide, acidic, acidic polysaccharide, activation, complex, construction, PAGE, reducing, reducing end, linear, glycosylation, stereoselective, PDF, lysoamidase

  NCBI PubMed ID: 15614860
  Publisher: Vch Verlagsgesellschaft
  Institutions: Leiden Institute of Chemistry Leiden University P.O. Box 9502, 2300 RA Leiden, The Netherlands, Fax: (+31) 715-274-307
  Methods: chemical synthesis
  
   
  
  Xanthomonas
  CSDB ID 10095 (all data & tools)

Show legend Show as text

Structure type: oligomer
Trivial name: acidic polysaccharide
Contained glycoepitopes: IEDB_135813,IEDB_137340,IEDB_141807,IEDB_151531

• Article ID: 1541
  Litjens RE, den Heeten R, Timmer MS, Overkleeft HS, van der Marel GA "An expedient synthesis of the repeating unit of the acidic polysaccharide of the bacteriolytic complex of lysoamidase" - Chemistry 11(3) (2005) 1010-1016
  

  The first synthesis of the trisaccharide repeating unit of the acidic polysaccharide of the bacteriolytic complex of lysoamidase is presented. The construction is based on a linear glycosylation strategy that starts from the reducing end and employs thio- and selenoglycosides in a highly stereoselective manner by a single set of activation conditions. The thus-formed trisaccharide is selectively deprotected and oxidised, after which a final deprotection step furnishes the desired repeating unit

  synthesis, chemistry, polysaccharide, repeating unit, trisaccharide, acidic, acidic polysaccharide, activation, complex, construction, PAGE, reducing, reducing end, linear, glycosylation, stereoselective, PDF, lysoamidase

  NCBI PubMed ID: 15614860
  Publisher: Vch Verlagsgesellschaft
  Institutions: Leiden Institute of Chemistry Leiden University P.O. Box 9502, 2300 RA Leiden, The Netherlands, Fax: (+31) 715-274-307
  Methods: chemical synthesis
  
   
  
  Xanthomonas
  CSDB ID 10302 (all data & tools)