191340-56-4

Upstream product

• 412909-27-4 9-((2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylamine 
• 108-93-0 cyclohexanol 
• 16838-89-4 2,3,5-tri-O-benzyl-D-ribofuranose 
• 13871-89-1 trimethylsilyl cyclohexyl ether 
• 58381-23-0 (3R,4R,5R)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-yl acetate 

Relevant academic research and scientific papers

Diphosphonium Salts as Effective Reagents for Stereoselective Synthesis of 1,2-cis-Ribofuranosides

1,2-cis-Ribofuranosides are stereoselectivly synthesized in high yields directly from 1-hydroxy sugars and alcohols or trimethylsilylated nucleophiles by the use of diphosphonium salts as a condensation reagent.

One-step syntheses of alkyl glycosides and alkyl-substituted DNA oligomers by chemoselective glycosidations using DNA bases

The simple and practical synthesis of alkyl glycosides by novel chemoselective glycosidations using natural resources, DNA and RNA nucleosides, was realized, and the one-step synthesis of chemoselectively modified DNA oligomers using the glycosidation met

Trityl salt catalyzed stereoselective glycosylation of alcohols with 1-hydroxyribofuranose

In the presence of a catalytic amount of several trityl salts, 2,3,5-tri-O-benzyl-D-ribofuranose smoothly reacted with alcohols to give various β-ribofuranosides in high yields with high stereoselectivity while reversed stereoselectivity was observed in t

Tin(II) Chloride Catalyzed Synthesis of Ribofuranosides

Catalytic synthesis of several D-ribofuranosides from 2,3,5-tri-O-benzyl-1-O-iodoacetyl-D-ribofuranose and trimethylsilylated nucleophiles such as 3β-cholestanyl trimethylsilyl ether and phenyl trimethylsilyl sulfide is efficiently promoted by tin(II) chl