135253-88-2

Upstream product

• 100-02-7 4-nitro-phenol 
• 2492-87-7 4-nitrophenyl-β-D-glucoside 
• 5987-78-0 p-nitrophenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyde 
• 42011-36-9 (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(4-aminophenoxy)-tetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 814-68-6 acryloyl chloride 
• 20818-25-1 4-aminophenyl β-D-glucopyranoside 
• 91255-92-4 Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-(4-acryloylamino-phenoxy)-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

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.