323195-45-5

Upstream product

• 106-45-6 para-thiocresol 
• 220645-20-5 p-methylphenyl 3,4,6-tri-O-acetyl-2-deoxy-1-thio-2-(2,2,2-trichloroethyloxycarbonylamino)-β-D-glucopyranoside 
• 122210-01-9 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-D-glucopyranose 
• 122210-05-3 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-β-D-glucopyranose 

Downstream Products

• 220645-30-7 p-methylphenyl 3,6-di-O-benzoyl-2-deoxy-1-thio-2-(2,2,2-trichloroethyloxycarbonylamino)-β-D-glucopyranoside 
• 323195-39-7 p-methylphenyl 2-deoxy-4,6-O-isopropylidene-2-(2,2,2-trichloroethoxycarbonylamino)-1-thio-β-D-glucopyranoside 
• 929040-52-8 p-tolyl N-2,2,2-trichloroethyloxycarbonyl-2-amino-4,6-O-benzylidene-2-deoxy-1-thio-β-D-glucopyranoside 
• 1038395-33-3 p-tolyl N-benzyl-2-amino-4,6-di-O-benzyl-2,3-N,O-carbonyl-2-deoxy-1-thio-β-D-glucopyranoside 
• 1038395-34-4 p-tolyl 2-amino-2,3-N,O-carbonyl-4,6-O-dibenzyl-2-deoxy-1-thio-β-D-glucopyranoside 
• 502692-37-7 Acetic acid (2R,4aR,6S,7R,8R,8aS)-2-phenyl-6-p-tolylsulfanyl-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl ester 
• 1453169-39-5 methyl (5-acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosyl)onate-(2→6)-N-benzyloxycarbonyl-5-aminopentyl 3,4-di-O-acetyl-6-O-tert-butyldimethylsilyl-2-deoxy-(2,2,2-trichloroethyloxycarbonyl)amino-β-D-glucosamine 
• 1453169-40-8 methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosyl)onate-(2→6)-N-benzyloxycarbonyl-5-aminopentyl 3,4-di-O-acetyl-6-O-tert-butyldimethylsilyl-2-deoxy-(2,2,2-trichloroethyloxycarbonyl)amino-β-D-glucosamine 
• 1453169-41-9 methyl (5-tert-butyloxycarbonyl-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosyl)onate-(2→6)-N-benzyloxycarbonyl-5-aminopentyl 3,4-di-O-acetyl-6-O-tert-butyldimethylsilyl-2-deoxy-(2,2,2-trichloroethyloxycarbonyl)-amino-β-D-glucosamine 
• 1453169-49-7 C₄₇H₆₅N₃O₂₃ 
• 1453169-50-0 (5-N-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosyl)onate-(2→6)-N-benzyloxycarbonyl-5-aminopentyl-2-deoxy-2-acetamido-β-D-glucosamine 
• 1453169-51-1 (5-N-benzyloxyacetamido-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosyl)onate-(2→6)-N-benzyloxycarbonyl-5-aminopentyl-2-deoxy-2-acetamido-β-D-glucosamine 
• 1453169-55-5 toluyl 3-O-(9-fluorenylmethoxycarbonyl)-6-O-tert-butyldimethylsilyl-2-deoxy-(2,2,2-trichloroethyloxycarbonyl)amino-1-thio-β-D-glucosamine 
• 1453169-67-9 N-benzyloxycarbonyl-5-aminopentyl 3,4-di-O-acetyl-6-O-tert-butyldimethylsilyl-2-deoxy-(2,2,2-trichloroethyloxycarbonyl)amino-β-D-glucosamine 

Relevant academic research and scientific papers

Differential Recognition of Deacetylated PNAG Oligosaccharides by a Biofilm Degrading Glycosidase

Exopolysaccharides consisting of partially de-N-acetylated poly-β-d-(1→6)-N-acetyl-glucosamine (dPNAG) are key structural components of the biofilm extracellular polymeric substance of both Gram-positive and Gram-negative human pathogens. De-N-acetylation

In situ formation of β-glycosyl imidinium triflate from participating thioglycosyl donors: Elaboration to disarmed-armed iterative glycosylation

β-Glycosyl imidinium triflate is generated from participating thioglycoside donors for disarmed-armed iterative glycosylations and one-pot oligosaccharide synthesis.

Stereoselectivity investigation on glycosylation of oxazolidinone protected 2-amino-2-deoxy-d-glucose donors based on pre-activation protocol

Diverse 2,3-oxazolidinone protected 2-amino-2-deoxy-d-glucose thioglycosides were prepared and studied as glycosyl donors at low temperature by BSM/Tf2O pre-activation protocol before the addition of glycosyl acceptors. The stereochemistry outc

Studies directed to the synthesis of oligochitosans - Preparation of building blocks and their evaluation in glycosylation studies

Thioglucosaminides with four different N-protecting groups, Troc, Phth, Alloc and PNZ could selectively be benzoylated at the C3 and C6-hydroxy groups in good yields without the requirement for low-temperature techniques. These reactions could be performe

Reactivity-based one-pot synthesis of the tumor-associated antigen N3 minor octasaccharide for the development of a photocleavable DIOS-MS sugar array

Sweet and light: Readily available thioglycosides with defined relative reactivity values were used as building blocks in a one-pot strategy to synthesize the tumor-associated carbohydrate antigen N3 minor (1). The target molecule was attached covalently to a porous silicon surface through a photocleavable linker for direct characterization in a mass spectrometer equipped with a laser source. (Chemical Equation Presented).

A new reactivity-based one-pot synthesis of N-acetyllactosamine oligomers

Poly-N-acetyllactosamine oligomer is a type-2 glycan core from which a number of important bioactive glycoconjugates are assembled in vivo. Development of an effective synthesis of N-acetyllactosamine oligomers will therefore provide a new chemoenzymatic

Synthesis of β-D-glucopyranosyl(1→3)-1-thiol-β-glucosamine disaccharide derivative as building block for the synthesis of hyaluronic acid

A practical synthetic method for the title disaccharide 2 is described. Glycosylation using thioglycoside as acceptor and glycosyl imidate as donor was performed with trimethylsilyltriflate as the promoter.

Programmable one-pot oligosaccharide synthesis

In an effort to develop a broadly applicable approach to the facile one- pot synthesis of oligosaccharides, the reactivity of a number of p- methylphenyl thioglycoside (STol) donors which are either fully protected or have one hydroxyl group exposed has b