381724-75-0

Upstream product

• 82598-84-3 2,3,4,6-tetra-O-benzyl-D-galactonolactone 
• 381724-74-9 ((3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester 

Downstream Products

• 849472-56-6 (S)-t-butyl 4-(2-((2S,3R,4S,5S,6R)-2-benzamido-3,4,5-tris(benzyloxy)-6-benzyloxymethyltetrahydro-2H-pyran-2-yl)acetamido)-2-(t-butoxycarbonylamino)butanoate 
• 381724-80-7 N-[(2S,3R,4S,5S,6R)-2-(Benzylcarbamoyl-methyl)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl]-benzamide 
• 849472-65-7 (S)-4-(2-((2S,3R,4S,5R,6R)-2-benzamido-3,4,5-tris(acetoxy)-6-acetoxymethyltetrahydro-2H-pyran-2-yl)acetamido)-2-(9-fluorenylmethoxycarbonylamino)butanoic acid 
• 849472-72-6 (S)-2-tert-Butoxycarbonylamino-4-[2-((2S,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-2-benzoylamino-tetrahydro-pyran-2-yl)-acetylamino]-butyric acid tert-butyl ester 

Relevant academic research and scientific papers

Access to unnatural glycosyl amino acid building blocks via a one-pot Ritter reaction

α-D-Galacto-2-deoxy-oct-3-ulopyranosonic acids, α-D-gluco-2- deoxy-oct-3-ulopyranosonic acids and α-L-galacto-2,8-dideoxy-oct-3- ulopyranosonic acids can be converted into unnatural glycosyl amino acids via a one-pot intramolecular Ritter reaction. Initia

One pot conversion of ketoses into sugar β-peptides via a ritter reaction

α-D-Galacto-2-deoxy-oct-3-ulopyranosonic acids can be converted into unnatural glycopeptides via a one pot intramolecular Ritter reaction. Initially, the ketopyranoside reacts under Lewis acid catalyzed conditions with a nitrile (aromatic or aliphatic) to