193
Views
10
CrossRef citations to date
0
Altmetric
Original Articles

SYNTHESIS OF A XYLOSYLATED RHAMNOSE PENTASACCHARIDE—THE REPEATING UNIT OF THE O-SPECIFIC SIDE CHAIN OF LIPOPOLYSACCHARIDES FROM THE REFERENCE STRAINS FOR Stenotrophomonas maltophilia SEROGROUP O18

&
Pages 89-97 | Received 17 Sep 2001, Accepted 02 Jan 2002, Published online: 28 Oct 2011

REFERENCES

  • Winn , A. M. and Wilkinson , S. G. 2001 . Structures of the O4 and O18 antigens of Stenotrophomonas maltophilia: a case of enantiomeric repeating units . Carbohydr. Res. , 330 : 215 – 221 .
  • Berg , G. , Roskot , N. and Smolla , K. 1999 . Antimicrobial treatment of pulmonary colonization and injection by Pseudomonas aeruginosa in cystic fibrosis patients . J. Clin. Microbiol. , 37 : 3594 – 3600 .
  • Juhasz , A. L. , Stanley , G. A. and Britz , M. L. 2000 . Microbial degradation and detoxification of high molecular weight polycyclic aromatic hydrocarbons by Stenotrophomonas maltophilia strain VUN 10,003 . Lett. Appl. Microbiol. , 30 : 396 – 401 .
  • Denton , M. , Keer , V. and Hawkey , P. M. 1998 . Clin. Correlation between genotype and lactamases of clinical and environmental strains of Stenotrophomonas maltophilia . Microbiol. Rev. , 11 : 57 – 80 .
  • Wang , W. and Kong , F. 1999 . Regio- and steroselective synthesis of mannose-containing oligosaccharides . Angew. Chem., Int. Ed. , 38 : 1247 – 1250 .
  • Wang , W. and Kong , F. 1998 . New synthetic methodology for regio- and stereoselective synthesis of oligosaccharides via sugar orthoester intermediates . J. Org. Chem. , 63 : 5744 – 5755 .
  • Du , Y. and Kong , F. 1999 . Regio- and stereoselective synthesis of rhamnose-containing oligosaccharides . J. Carbohydr. Chem. , 18 : 655 – 664 .
  • Zhu , Y. and Kong , F. 2000 . Synthesis of 1→6-linked mannose dodecasaccharide and glucose octasaccharide using glycosyl imidates as the donor and unprotected and partially protected sugars as the acceptors . Synlett , 5 : 663 – 669 .
  • Zhu , Y. and Kong , F. 2001 . A facile and effective synthesis of α-(1→6)-linked mannose di-, tri-, tetra-, hexa-, octa-, and dodecasaccharides and β-(1→6)-linked glucose di-, tri-, tetra-, hexa-, and octasaccharides using sugar trichloroacetimidates as the donors and unprotected or partially protected glycosides as the acceptors . Carbohydr. Res. , 332 : 1 – 21 .
  • Wang , W. and Kong , F. 1999 . A highly efficient and convergent synthesis of a hexasaccharide, a dimer of the repeating unit of the O2 antigen polysaccharide of Stenotrophomonas maltophilia . Carbohydr. Res. , 315 : 128 – 136 .
  • Mikkelsen , G. , Christensen , T. V. , Bols , M. , Lundt , I. and Sierks , M. R. 1995 . Aglycon mimicking: glycoside bond cleavage transition state mimics based on hydroxypyrrolidine inhibitors . Tetrahedron Lett. , 36 : 6541 – 6544 .
  • Vansteijn , A.M. P. , Kamerling , J. P. and Vliegenthart , J.F. G. 1991 . Synthesis of a spacer-containing repeating unit of the capsular polysaccharide of Streptococcus pneumoniae type 23F . Carbohydr. Res. , 211 : 261 – 277 .

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.