139189-60-9

Upstream product

• 592-04-1 mercury(II) cyanide 
• 75172-84-8 2,3,5-tri-O-benzyl-1-O-(p-nitrobenzoyl)-α,β-D-ribofuranose 
• 7677-24-9 trimethylsilyl cyanide 
• 91110-24-6 Acetic acid (2S,3R,4R,5R)-3,4-bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl ester 
• 139189-61-0 2,3,4,6-tetra-O-benzyl-D-xylo-hex-5-ulosononitrile 
• 86496-30-2 (2S,3R,4R,5R)-2,3,4,6-tetrakis(benzyloxy)-5-hydroxyhexanal oxime 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 139189-57-4 2,3,4,6-tetra-O-benzyl-D-glucononitrile 

Downstream Products

• 42890-06-2 (2R,3R,4R,5R)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-carboxylic acid 
• 138809-95-7 2,3,5-tri-O-benzyl-α-D-ribofuranosylmethanoic acid 
• 119155-79-2 ((2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-ylmethyl)-phosphoramidic acid methyl ester phenyl ester 
• 119155-79-2 ((2S,3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-ylmethyl)-phosphoramidic acid methyl ester phenyl ester 
• 119155-79-2 1-deoxy-1-<(methoxyphenoxyphosphonyl)amino>-3,4,6-tri-O-benzyl-2,5-anhydro-D-glucitol 
• 136409-55-7 methyl 2-(2',3',5'-tri-O-benzyl-β-D-ribofuranosyl)isonicotinate 
• 136409-54-6 methyl 2-(2',3',5'-tri-O-benzyl-α-D-ribofuranosyl)isonicotinate 
• 136409-53-5 4-methyl-2-(2',3',5'-tri-O-benzyl-β-D-ribofuranosyl)quinoline 
• 136409-52-4 4-methyl-2-(2',3',5'-tri-O-benzyl-α-D-ribofuranosyl)quinoline 
• 501101-30-0 diethyl (4R)-2-(2',3',5'-tri-O-benzyl-β-D-ribofuranosyl)-1,4-dihydro-6-methyl-4-[2-(trifluoromethyl)phenyl]pyridine-3,5-dicarboxylate 
• 501101-28-6 diethyl (4S)-2-(2',3',5'-tri-O-benzyl-β-D-ribofuranosyl)-1,4-dihydro-6-methyl-4-[2-(trifluoromethyl)phenyl]pyridine-3,5-dicarboxylate 
• 421554-04-3 diethyl (4S)-2-(2',3',5'-tri-O-benzyl-β-D-ribofuranosyl)-1,4-dihydro-6-methyl-4-phenylpyridine-3,5-dicarboxylate 
• 421554-03-2 diethyl (4R)-2-(2',3',5'-tri-O-benzyl-β-D-ribofuranosyl)-6-methyl-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate 

Relevant academic research and scientific papers

Stereoselective 1,2-cis Glycosylation Reaction of 1-O-Acetylribose with Silylated Nucleophiles by the Promotion of a New Catalyst System

1,2-cis-Ribofuranosides are stereoselectively prepared in high yields by the reaction of 1-O-acetyl-β-D-ribose with silylated nucleophiles by the promotion of a new catalyst system, the combined use of a catalytic amount of tin(IV) chloride and tin(II) tr

4-AMINO-3-(2,3,5-TRI-O-BENZYL-β-D-RIBOFURANOSYL)-5-PYRAZOLECARBONITRILE. SYNTHESIS AND CONVERSION INTO A SUGAR-BLOCKED 5,7-DISUBSTITUTED FORMYCIN ANALOG

The title compound, a potential intermediate to protected C-nucleoside analogs related to formycin A, was synthesized via a new route wherein 2,3,5-tri-O-benzyl-1-O-(p-nitrophenyl)-D-ribofuranose was converted to 2,5-anhydro-3,4,6-tri-O-benzyl-D-allonic a