848034-51-5

Upstream product

• 286369-06-0 2,6-anhydro-3,4,5,7-tetra-O-benzoyl-D-glycero-D-gulo-heptonamide 
• 120297-35-0 (1S)-tetra-O-benzoyl-1-(4-methoxy-phenyl)-1,5-anhydro-D-glucitol 
• 286369-05-9 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl cyanide 

Downstream Products

• 848034-59-3 2,2,2-trichloroethyl 2,6-anhydro-3,4,5,7-tetra-O-benzoyl-D-glycero-D-gulo-heptonate 
• 848034-55-9 tert-butyl 2,6-anhydro-3,4,5,7-tetra-O-benzoyl-D-glycero-D-gulo-heptonate 
• 1430730-66-7 5-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-3-(3,4,5-trimethoxyphenyl)-1,2,4-triazole 

Relevant academic research and scientific papers

Cyanide-Free Synthesis of Glycosyl Carboxylic Acids and Application for the Synthesis of Scleropentaside A

We have developed a cyanide-free strategy for the synthesis of glycosyl carboxylic acids, which can provide 1,2-trans or 1,2-cis glycosyl carboxylic acids and is compatible with common protecting groups. The synthetic utility was demonstrated by the synth

Synthesis of substituted 2-(β-d-glucopyranosyl)-benzimidazoles and their evaluation as inhibitors of glycogen phosphorylase

Microwave assisted condensation of O-perbenzoylated C-(β-d- glucopyranosyl)formic acid with 1,2-diaminobenzenes in the presence of triphenylphosphite gave the corresponding O-protected 2-(β-d- glucopyranosyl)-benzimidazoles in moderate yields. O-Perbenzoy

Anomeric α-azido acid (2-azido-2-deoxy-hept-2-ulopyranosonic acid) derivatives en route to peptides incorporating sugar amino acids

Per-O-acylated 2,6-anhydro-aldoheptonic acids of d-glycero-d-gulo and d-glycero-l-manno configuration obtained by nitrosation of the corresponding aldonamides were transformed into methyl-, tert-butyl-, 2,2,2-trichloroethyl-, and pentachlorophenyl esters,