652993-94-7

Upstream product

• 268725-01-5 3-(2'-N-acetylamino-3',4',6'-tri-O-benzyl-2'-deoxy-β-D-glucopyranosyl)-1-propene 
• 262286-48-6 3-(2'-N-acetylamino-3',4',6'-tri-O-benzyl-2'-deoxy-α-D-glucopyranosyl)-1-propene 
• 214193-76-7 1-(2'-acetamido-2'-deoxy-α-D-glucopyranosyl)-2-propene 
• 180778-36-3 3-(2'-acetamido-3',4',6-tri-O-acetyl-2'-deoxy-α-D-glucopyranosyl)-1-propene 
• 180980-29-4 5-acetamido-6,7,9-tri-O-acetyl-4,8-anhydro-1,2,3,5-tetradeoxy-D-glycero-D-ido-non-enitol 
• 180778-41-0 3-(2'-N-acetylamino-2'-deoxy-β-D-glucopyranosyl)-1-propene 
• 537031-63-3 (E)-1-(2'-N-acetylamino-3',4',6'-tri-O-benzyl-2'-deoxy-α-D-glucopyranosyl)-2-propene 
• 100-39-0 benzyl bromide 
• 898803-24-2 2-(2'-N-acetylamido)-(2'-deoxy-3',4',6'-tri-O-acetyl-β-D-glucopyranosyl)-1,3-bis(phenylmethyl)imidazolidine 
• 898803-22-0 1-(2'-N-acetylamino)-(2'-deoxy-3',4',6'-tri-O-acetyl-β-D-glucopyranosyl)propane-2-one 
• 898803-23-1 2-(N-acetylamido)-2-deoxy-1-formyl-3,4,6-tri-O-acetyl-β-D-glucopyranoside 
• 853269-37-1 1-C-(2-N-acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranosyl)-propane-2-one 
• 898803-27-5 2-(2'-N-acetyl)-(2'-deoxy-3',4',6'-tri-O-benzyl-β-D-glucopyranosyl)-1,3-bis(phenylmethyl)imidazolidine 
• 578729-63-2 N-[(2S,3S,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((E)-propenyl)-tetrahydro-pyran-3-yl]-acetamide 

Downstream Products

• 182618-25-3 3-acetamido-2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-glycero-D-gulo-heptonic acid 

Relevant academic research and scientific papers

A short synthetic route to β-C-glycosides of N-acetylglucosamine

A short and efficient process is described for the synthesis of protected and unprotected 1-formyl-C-glycosides of N-acetylglucosamine. Georg Thieme Verlag Stuttgart.

New and general synthesis of β-C-glycosylformaldehydes from easily available β-C-glycosylpropanones

A highly effective method for the introduction of a formyl group at the anomeric position of pyranosides was developed via enolisation of β-C-d-glycopyranosylpropan-2-one using thermodynamic conditions then oxidative cleavage of the more substituted doubl

Synthesis of α- and β-C-glycosides of N-acetylglucosamine

As part of efforts to make available new classes of bioactive C-glycoconjugates, D-glucosamine has been effectively converted into a series of 2-deoxy-2-amino-C-glycosides. This versatile approach is keyed by a remarkably effective metal catalyzed olefin isomerization of the isomeric C-allyl amino sugars which, in turn, are readily available via radical allylation of D-glucosamine.

Synthesis of C-Glycosyl Phosphate and Phosphonate, Analogues of N-Acetyl-α-D-Glucosamine 1-Phosphate

Synthesis of α-C-ethylene phosphate and phosphonate as well as α-C-methylene phosphate analogues of N-acetyl-α-D-glucosamine 1-phosphate is reported starting from the common perbenzylated 2-acetamido-2-deoxy-α-C-allyl glucoside. Anomerisation of the corre