527680-93-9

Upstream product

• 828930-34-3 p-tolyl 2,3,5-tri-O-acetyl-1-thio-β-D-xylofuranoside 
• 828930-37-6 p-tolyl 1-thio-β-D-xylofuranoside 
• 42927-46-8 tetra-O-acetyl-D-xylofuranose 
• 106-45-6 para-thiocresol 
• 98-88-4 benzoyl chloride 
• 828930-45-6 p-tolyl 2,3-anhydro-1-thio-β-D-ribofuranoside 

Downstream Products

• 527681-84-1 methyl 5-O-(2,3-anhydro-5-O-benzoyl-α-D-ribofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside 
• 527681-88-5 methyl 6-O-(2,3-anhydro-5-O-benzoyl-α-D-ribofuranosyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 402759-03-9 methyl 5-O-(2-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside 

Relevant academic research and scientific papers

An efficient route to thioglycosides with the 2,3-anhydro-D-ribo stereochemistry

An improved route for the synthesis of p-tolyl 2,3-anhydro-5-O-benzoyl-1- thio-β-d-ribofuranoside and its α anomer, which are important intermediates in the synthesis of α- and β-d-arabinofuranosides, has been developed. The products are obtained in six steps from d-xylose in 39% overall yield.

2,3-Anhydro sugars in glycoside bond synthesis. Highly stereoselective syntheses of oligosaccharides containing α- and β-arabinofuranosyl linkages

The ever-increasing discovery of biologically important events mediated by carbohydrates has generated great interest in the synthesis of oligosaccharides and the development of new methods for glycosidic bond formation. In this paper, we report that 2,3-