135253-87-1

Upstream product

• 100-02-7 4-nitro-phenol 
• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 
• 13089-27-5 p-nitrophenyl 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranoside 
• 65907-85-9 p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-D-glucopyranoside 
• 3459-18-5 4-nitrophenyl N-acetyl-β-D-glucosaminide 
• 14419-59-1 4-aminophenyl 2-(acetylamino)-2-deoxy-β-D-glucopyranoside 
• 814-68-6 acryloyl chloride 
• 79-10-7 acrylic acid 
• 135253-85-9 Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester 

Relevant academic research and scientific papers

CHEMO-ENZYMATIC SYNTHESIS OF A GLYCOPOLYMER CARRYING CLUSTERED-N-ACETYL-Β-LACTOSAMINE MOIETIES

A polyacrylamide derivative having a β-linked N-acetyllactosamine moiety, a major component of oligosaccharide chains of glycoproteins, on each repeating unit was synthesized via a chemo-enzymatic process. p-Nitrophenyl N-acetyl-β-lactosaminide was prepar

Syntheses and Transformations of Glycohydrolase Substrates into Protein Conjugates Based on Michael Additions

The glycosyl chloride 1 and bromides 2 and 3 were stereospecifically transformed into p-nitrophenyl glycosides by phase transfer catalysis; these glycohydrolase substrates were reduced and N-acryloylated to afford Michael acceptors which reacted with amine functions of proteins.