41341-59-7

Upstream product

• 106-54-7 p-Chlorothiophenol 
• 36868-85-6 4-chlorophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-galactopyranoside 

Downstream Products

• 296769-13-6 4-chlorophenyl 4,6-O-benzylidene-1-thio-β-D-galactopyranoside 
• 296769-00-1 4-chlorophenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside 
• 296768-97-3 4-chlorophenyl 2,3-di-O-benzyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside 
• 1352306-76-3 C₂₆H₃₃ClO₆S 
• 1352306-73-0 p-chlorophenyl 2-O-benzyl-1-thio-β-D-galactopyranoside 
• 1352306-79-6 p-chlorophenyl 2-O-benzyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside 
• 1352306-82-1 p-chlorophenyl 3-O-acetyl-2-O-benzyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside 
• 1186201-47-7 C₃₉H₄₁ClO₈SSi 
• 1186201-46-6 4-chlorophenyl (5-acetamido-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-2-nonulopyranosylonate)-(2->6)-6-deoxy-1,6-dithio-β-D-galactopyranoside 
• 1186201-49-9 C₃₄H₂₆ClF₃O₁₀S₂ 
• 1186201-48-8 4-chlorophenyl 2,3,4-tri-O-benzoyl-1-thio-β-D-galactopyranoside 
• 1057491-23-2 4-chlorophenyl 3,4-O-isopropylidene-1-thio-β-D-galactopyranoside 

Relevant academic research and scientific papers

Total synthesis of LeA-LacNAc pentasaccharide as a ligand for Clostridium difficile toxin A

The toxins TcdA and TcdB produced by the human pathogen Clostridium difficile gain entrance to host epithelial cells by recognizing cell-surface carbohydrate ligands. Inhibiting the attachment of these toxins to host cells has been proposed to be a viable

Stereoselective iterative one-pot synthesis of N-glycolylneuraminic acid-containing oligosaccharides

(Chemical Equation Presented) The use of an N-acyloxazolidinone-protected S-adamantanyl thiosialoside allows the highly stereoselective, one-pot multicomponent synthesis of α-slaloside-based oligosaccharides.

A convenient preparation of glycosyl chlorides from aryl/alkyl thioglycosides

(equation presented) Because of the vast structural diversity encountered in the field of glycobiology, versatile methods for orthogonal oligosaccharide assembly are always of interest. Reported herein is the preparation of glycosyl chloride donors obtained by reaction of the corresponding thioglycoside precursors with chlorosulfonium chloride reagent 4. The crude chlorides thus obtained can be used directly in subsequent glycosylation reactions, and examples of the generality of this approach are provided.