72402-15-4

Upstream product

• 4099-85-8 methyl 2,3-O-isopropylidene-D-ribofuranoside 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 

Downstream Products

• 78038-31-0 Methyl 5-O-benzyl-α,β-D-ribofuranoside 
• 871578-65-3 (2'R,3'S,4'R)-1-(2'-benzyloxymethyl-3'-hydroxytetrahydrofuran-4'-yl)-3-aminocarbonyl-1,2,4-triazole 
• 871578-63-1 (2'R,3'S,4'R)-1-(2'-benzyloxymethyl-3'-hydroxytetrahydrofuran-4'-yl)-3-methoxycarbonyl-1,2,4-triazole 
• 1054610-75-1 (3aR,4R,6aS)-4-Benzyloxymethyl-tetrahydro-furo[3,4-d][1,3,2]dioxathiole 2,2-dioxide 
• 871578-58-4 (3aR,4R,6aS)-4-Benzyloxymethyl-tetrahydro-furo[3,4-d][1,3,2]dioxathiole 2-oxide 
• 871578-57-3 1,4-anhydro-5-O-benzyl-D-ribitol 

Relevant academic research and scientific papers

Synthesis and biological evaluation of novel isonucleosides with 1,2,4-triazole-3-carboxamide

Novel 1,2,4-triazole isonucleosides (1 and 2) were efficiently synthesized starting from D-ribose and D-xylose, respectively. The key steps were condensation of cyclic sulfate 8 with methyl-1,2,4-triazole-3-carboxylate and nucleophilic displacement of the

SYNTHESIS OF FOUR STEREOISOMERS OF 4-AMINO-2-(HYDROXY-METHYL)TETRAHYDROFURAN-4-CARBOXYLIC ACID

The 5-benzyl ether, 15, of a 1,2,,4,5-pentanetetrol of known 2S configuration was made by a multistep synthesis from D-ribose.Ring-closure of the 1-O-otosyl derivative, 17, with retention of configuration, followed by oxidation, gave the 2S enantiomer, 22