849472-65-7

Upstream product

• 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 
• 381724-75-0 ((3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-acetic acid 
• 381724-76-1 (6S,8R,9S,10S,11R)-9,10,11-Tris-benzyloxy-8-benzyloxymethyl-2-phenyl-3,7-dioxa-1-aza-spiro[5.5]undec-1-en-4-one 
• 400888-39-3 ((2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester 
• 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 
• 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 
• 88744-04-1 (9-fluorenyl)methyl pentafluorophenyl carbonate 

Relevant academic research and scientific papers

Ritter-based glycoconjugation of amino acids and peptides-access to novel glycoconjugates displaying a β-amide linkage between amino acid and sugar moiety

β-Peptidic-d-gluco-, d-galacto-, and l-fuco-configured glycosyl amino acids can be prepared from the corresponding 2-deoxy-oct-3-ulopyranosonic acids via a one-pot intramolecular Ritter reaction. Initially, a ketopyranoside-based acid condenses under Lewi

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