637741-83-4

Upstream product

• 78158-90-4 (5R)-5-<(triphenylmethoxy)methyl>-γ-butyrolactone 
• 76-83-5 trityl chloride 
• 52813-63-5 (5R)-2,3,4,5-tetrahydro-5-hydroxymethyl-2-furanone 

Downstream Products

• 148440-97-5 (5R)-4,5-Dihydro-5-<(triphenylmethoxy)methyl>furan 
• 148553-57-5 2,4-dimethoxy-(2'R)-trans-5-<2',5'-dihydro-5'-<(triphenylmethoxy)methyl>-2'-furanyl>pyrimidine 
• 148441-01-4 2,4-dimethoxy-(2'R)-5-<2',3'-dihydro-5'-<(triphenylmethoxy)methyl>-2'-furanyl>pyrimidine 

Relevant academic research and scientific papers

Syntheses of 2′,3′-dideoxy-L-glyceropentofuranosyl C-nucleosides

2′,3′-Dideoxy-L-C-nucleosides, 4-amino-8-(2,3-dideoxy-L-glyceropentofuranosyl)pyrazolo[1,5-a]-1,3,5-triazines (9 and 10), 4-amino-7-(2,3-dideoxy-L-glyceropentofuranosyl)-3H,5H-pyrrolo[3,2-d]pyrimidines (17 and 18), 7-(2,3-dideoxy-L-glyceropentofuranosyl)-

Enantio- and Diastereoisomers of 2,4-Dimethoxy-5-(2,3-dideoxy-5-O-tritylribofuranosyl)pyrimidine. 2',3'-Dideoxy Pyrimidine C-Nucleosides by Palladium-Mediated Glycal-Aglycon Coupling

Newly available enantiomeric 2,3-dideoxy glycals, (5S)- and (5R)-4,5-dihydro-5-furans and 2,4-dimethoxy-5-iodopyrimidine undergo palladium-mediated coupling by two different, complementary procedures to form enantiomeric pairs of