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
Structures of the O4 and O18 antigens of Stenotrophomonas maltophilia: A case of enantiomeric repeating units
Winn, A.M.; Wilkinson, S.G. Structures of the O4 and O18 antigens of Stenotrophomonas maltophilia: a case of enantiomeric repeating units. Carbohydr. Res. 2001, 330, 215-221.
Antimicrobial treatment of pulmonary colonization and injection by Pseudomonas aeruginosa in cystic fibrosis patients
Berg, G.; Roskot, N.; Smolla, K. Antimicrobial treatment of pulmonary colonization and injection by Pseudomonas aeruginosa in cystic fibrosis patients. J. Clin. Microbiol. 1999, 37, 3594-3600.
Microbial degradation and detoxification of high molecular weight polycyclic aromatic hydrocarbons by Stenotrophomonas maltophilia strain VUN 10,003
Juhasz, A.L.; Stanley, G.A.; Britz, M.L. Microbial degradation and detoxification of high molecular weight polycyclic aromatic hydrocarbons by Stenotrophomonas maltophilia strain VUN 10,003. Lett. Appl. Microbiol. 2000, 30, 396-401.
Clin. correlation between genotype and lactamases of clinical and environmental strains of Stenotrophomonas maltophilia
Denton, M.; Keer, V.; Hawkey, P.M. Clin. Correlation between genotype and lactamases of clinical and environmental strains of Stenotrophomonas maltophilia. Microbiol. Rev. 1998, 11, 57-80.
New synthetic methodology for regio- and stereoselective synthesis of oligosaccharides via sugar orthoester intermediates
Wang, W.; Kong, F. New synthetic methodology for regio- and stereoselective synthesis of oligosaccharides via sugar orthoester intermediates. J. Org. Chem. 1998, 63, 5744-5755.
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
Zhu, Y.; Kong, F. 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 2000, 5, 663-669.
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
Zhu, Y.; Kong, F. 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. 2001, 332, 1-21.
A highly efficient and convergent synthesis of a hexasaccharide, a dimer of the repeating unit of the O2 antigen polysaccharide of Stenotrophomonas maltophilia
Wang, W,; Kong, F. 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. 1999, 315, 128-136.
Aglycon mimicking: Glycoside bond cleavage transition state mimics based on hydroxypyrrolidine inhibitors
Mikkelsen, G.; Christensen, T.V.; Bols, M.; Lundt, I.; Sierks, M.R. Aglycon mimicking: glycoside bond cleavage transition state mimics based on hydroxypyrrolidine inhibitors. Tetrahedron Lett. 1995, 36, 6541-6544.
Synthesis of a spacer-containing repeating unit of the capsular polysaccharide of Streptococcus pneumoniae type 23F
Vansteijn, A.M.P.; Kamerling, J.P.; Vliegenthart, J.F.G. Synthesis of a spacer-containing repeating unit of the capsular polysaccharide of Streptococcus pneumoniae type 23F. Carbohydr. Res. 1991, 211, 261-277.