929040-52-8

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 323195-45-5 p-methylphenyl 2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-1-thio-β-D-glucopyranoside 
• 220645-20-5 p-methylphenyl 3,4,6-tri-O-acetyl-2-deoxy-1-thio-2-(2,2,2-trichloroethyloxycarbonylamino)-β-D-glucopyranoside 

Downstream Products

• 502692-38-8 tolyl 3-O-acetyl-6-O-benzyl-2-deoxy-2-trichloroethoxycarbonylamino-1-thio-β-D-glucopyranoside 
• 502692-47-9 4-Oxo-pentanoic acid (2S,3R,4S,5R,6R)-2-[(2R,3S,4R,5R,6S)-4-acetoxy-2-benzyloxymethyl-6-p-tolylsulfanyl-5-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-3-yloxy]-5-benzyloxy-6-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-3-yl ester 
• 502692-46-8 4-oxo-pentanoic acid 2-[4-acetoxy-2-benzyloxymethyl-6-p-tolylsulfanyl-5-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-3-yloxy]-5-benzyloxy-6-benzyloxymethyl-4-(4-methoxy-benzyloxy)-tetrahydro-pyran-3-yl ester 
• 905267-00-7 p-tolyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-1-thio-2-(2,2,2-trichloroethoxy)carbamoylamino-β-D-glucopyranoside 
• 502692-44-6 p-tolyl 3,6-di-O-benzyl-2-deoxy-1-thio-2-(2,2,2-trichloroethoxy)carbamoylamino-β-D-glucopyranoside 
• 1407151-68-1 C₃₀H₂₈Cl₃NO₇S 
• 1407151-96-5 p-tolyl 6-O-[3,4,6-tri-O-acetyl-2-(2,2,2-trichloroethoxycarbonylamino)-2-deoxy-β-D-glucopyranosyl]-3-O-benzoyl-4-O-benzyl-2-(2,2,2-trichloroethoxycarbonylamino)-2-deoxythio-β-D-glucopyranoside 
• 1407151-69-2 p-tolyl 2-O-benzoyl-2-O-benzyl-2-(2,2,2-trichloroethoxycarbonylamino)-2-deoxythio-β-D-glucopyranoside 
• 1391598-09-6 4-methyphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-o-trifluoromethylbenzylideneamino-α-D-glucopyranosyl-(1→3)-4,6-O-benzylidene-2-deoxy-2-(2,2,2-trichloroethyl)amino-1-thiol-β-D-glucopyranoside 
• 1391598-10-9 4-methyphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-o-trifluoromethylbenzylideneamino-β-D-glucopyranosyl-(1→3)-4,6-O-benzylidene-2-deoxy-2-(2,2,2-trichloroethyl)amino-1-thiol-β-D-glucopyranoside 

Relevant academic research and scientific papers

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

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