13245-34-6

Upstream product

• 51223-74-6 N-(N-benzyloxycarbonylglycyl)-tetra-O-acetyl-β-D-glucopyranosylamine 
• 20379-59-3 D-glucopyranosyl azide 
• 1202249-77-1 N-(benzyloxycarbonyl)glycine 2-(diphenylphosphanyl)-4-fluorophenyl ester 
• 7284-37-9 D-glucopyranosyl amine 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 15050-24-5 N-(benzyloxycarbonyl)glycyl chloride 

Downstream Products

• 51223-74-6 N-(N-benzyloxycarbonylglycyl)-tetra-O-acetyl-β-D-glucopyranosylamine 

Relevant academic research and scientific papers

GLYCOAMINO ACID AND USE THEREOF

An object of the present invention is to provide an amino acid precursor which shows improvement in the properties (particularly water-solubility, stability in water, bitter taste etc.) of amino acid, and can be converted to amino acid in vivo etc. The present invention relates to a compound for an amino acid precursor, which is a compound represented by the formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof.

Stereoselective synthesis of N-glycosyl amino acids by traceless Staudinger ligation of unprotected glycosyl azides

The stereoconservative Staudinger ligation of unprotected α- and β-glycosyl azides with 2-(diphenylphosphanyl)-4fluorophenyl esters to afford α- and β-N-glycosyl amino acids is described. The ligation method works reliably well for unprotected β-azides of