228115-93-3

Upstream product

• 52443-07-9 3,4,5,7-tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptonitrile 
• 89064-71-1 β-C-(hydroxymethyl)-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 
• 98-59-9 p-toluenesulfonyl chloride 
• 89064-74-4 (2,3,4,6-tetra-O-benzyl-β-D-mannopyranosyl)methanol 
• 228115-89-7 1,3-diphenyl-2-(2,3,4-tri-O-benzyl-6-O-triphenylmethyl-β-D-galactopyranosyl)-imidazolidine 
• 228115-88-6 1,3-diphenyl-2-(6-O-triphenylmethyl-β-D-galactopyranosyl)-imidazolidine 
• 71420-08-1 1,3-diphenyl-2-(tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptosyl)imidazolidine 
• 228115-90-0 2,6-anhydro-3,4,5-tri-O-benzyl-L-glycero-L-galacto-heptitol 

Relevant academic research and scientific papers

Synthesis of hexopyranosyl pyrimidine homonucleosides

A simple and convenient methodology has been developed for the synthesis of novel hexopyranosyl pyrimidine homonucleosides and hexopyranosyl double-headed pyrimidine homonucleosides from the corresponding native sugars, d-glucose and d-mannose. Thus, hexo

Synthesis studies of structural analogues of tagetitoxin: 4-O-acetyl-3- amino-1,6-anhydro-3-deoxy-D-gulose 2-phosphate

Synthetic approaches to structural analogues of tagetitoxin (1) are described. The successful route to analogue 3 (X=O) has, as a key step, protection of the cis-vicinal amino alcohol moiety of compound 7 as an N- benzylated cyclic carbamate (9). X-Ray cr