174272-04-9

Upstream product

• 20766-85-2 N-acryloyl-6-aminohexanoic acid 
• 174272-03-8 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-[6-((S)-2-amino-3-phenyl-propionylamino)-hexyloxy]-tetrahydro-pyran-4-yl ester 
• 60-32-2 6-aminohexanoic acid 
• 1161-13-3 N-Cbz-L-Phe 
• 174272-02-7 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-[6-((S)-2-benzyloxycarbonylamino-3-phenyl-propionylamino)-hexyloxy]-tetrahydro-pyran-4-yl ester 
• 174272-11-8 6-(N-benzyloxycarbonyl L-phenylalanyl)-amino-1-hexanol 
• 4048-33-3 6-amino-1-hexanol 

Downstream Products

• 174272-05-0 6-Acryloylamino-hexanoic acid {(S)-1-[6-((2R,3R,4R,5S,6R)-3-acetylamino-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-hexylcarbamoyl]-2-phenyl-ethyl}-amide 

Relevant academic research and scientific papers

High performance polymer supports for enzyme-assisted synthesis of glycoconjugates

Efficient and practical methodology for the construction of carbohydrates, including oligosaccharide derivatives and sphingoglycolipids, was established on the basis of a watersoluble polymer supports having unique linkers that can be cleaved by specific

An Efficient Synthesis of Sialoglycoconjugates on a Peptidase-Sensitive Polymer Support

A novel method for the enzymatic synthesis of oligosaccharide derivatives on a α-chymotrypsin-sensitive polymer support is described.The primer polymer having N-acetyl-D-glucosamine (GlcNAc) residue through a phenylalanine-containing spacer moiety was successfully elongated with galactosyl and sialyltransferases to give a glycopolymer bearing sialyl α(2->) N-acetyllactosamine branches in high yield.Subsequent hydrolysis with α-chymotripsin proceeded smoothly and afforded a versatile sialotrisaccharide derivative having a terminal amino group which can be used for creating neoglycoconjugates.