195192-36-0

Upstream product

• 32934-24-0 S-ethyl 2,3,4,6-tetra-O-acetyl-1-deoxy-1-thio-α-D-mannopyranoside 
• 195192-34-8 ethyl 4-O-benzyl-2,3-O-isopropylidene-1-thio-6-O-trityl-α-D-mannopyranoside 
• 195192-33-7 ethyl 2,3-O-isopropylidene-1-thio-6-O-triphenylmethyl-α-D-mannopyranoside 
• 128850-48-6 ethyl 1-thio-6-O-triphenylmethyl-α-D-mannopyranoside 
• 7473-36-1 ethyl 1-thio-α-D-mannopyranoside 
• 195192-35-9 ethyl 4-O-benzyl-2,3-O-isoproylidene-1-thio-α-D-mannopyranoside 

Downstream Products

• 195192-37-1 (R)-1-((3aS,4R,6R,7S,7aS)-7-Benzyloxy-4-ethylsulfanyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl)-2-(dimethyl-phenyl-silanyl)-ethanol 
• 1240564-06-0 ethyl 4,7-di-O-benzyl-2,3-O-isopropylidene-1-thio-D-glycero-α-D-manno-heptopyranoside 
• 1240564-07-1 ethyl 4,7-di-O-benzyl-2,3-O-isopropylidene-1-thio-L-glycero-α-D-manno-heptopyranoside 

Relevant academic research and scientific papers

Chemical Synthesis and Immunological Evaluation of Helicobacter pylori Serotype O6 Tridecasaccharide O-Antigen Containing a dd-Heptoglycan

The development of glycoconjugate vaccines against Helicobacter pylori is challenging. An exact epitope of the H. pylori lipo-polysaccharide (LPS) O-antigens that contain Lewis determinant oligosaccharides and unique dd-heptoglycans has not yet been ident

Synergistic Glycosylation as Key to the Chemical Synthesis of an Outer Core Octasaccharide of Helicobacter pylori

Helicobacter pylori, a widespread gastric bacterial pathogen that infects 90 % of the population in developing countries, causes chronic gastritis, peptic ulcers and gastric cancer. Battling H. pylori infection is a serious challenge due to the increased

Synthesis of phosphorylated 3,4-branched trisaccharides corresponding to LPS inner core structures of Neisseria meningitidis and Haemophilus influenzae

2-(N-Benzyloxycarbonyl)aminoethyl 7-O-acetyl-6-O-allyl-2-O-benzoyl-4-O- benzyl-3-O-chloroacetyl-Lglycero- α-D-manno-heptopyranosyl-(1→3)-[2, 3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1→4)]-6,7-di-O-acetyl-2-O- benzyl-L-glycero-α-D-manno-heptopyranoside, a

Synthesis of a trisaccharide fragment corresponding to the lipopolysaccharide region of vibrio parahaemolyticus

Vicinal syn-dihydroxylation of D-manno-hept-6-enopyranosides 4 and 10 with OsO4 afforded D-glycero-α-D-manno-heptopyranosides 5 and 11, respectively, in good yield and with a high degree of stereoselectivity. Compound 5 was converted into DD-He