73864-50-3

Upstream product

• 73864-46-7 3-C-ethyl-1,2-O-isopropylidene-α-D-allofuranose 
• 39707-80-7 3-C-ethyl-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 155470-62-5 5-O-tert-butyldimethylsilyl-1,2-O-isopropylidene-3-C-(2-trimethylsilylethynyl)-α-D-ribofuranose 
• 155470-63-6 3-C-ethynyl-1,2-O-isopropylidene-α-D-ribo-pentofuranose 
• 98-88-4 benzoyl chloride 
• 73864-48-9 3-C-ethyl-1,2-O-isopropylidene-α-D-ribofuranose 

Downstream Products

• 80581-76-6 1,2,3-tri-O-acetyl-5-O-benzoyl-3-C-ethyl-α,β-D-ribofuranose 
• 73864-54-7 1-(2,3-di-O-acetyl-5-O-benzoyl-3-C-ethyl-β-D-ribofuranosyl)uracyl 
• 211113-58-5 C₃₂H₂₉N₃O₈ 
• 211113-64-3 C₃₂H₂₈N₂O₉ 
• 211113-56-3 1,2,3,5-tetra-O-benzoyl-3-C-ethyl-α,β-D-ribo-pentofuranose 

Relevant academic research and scientific papers

Nucleosides and nucleotides, 175. Structural requirements of the sugar moiety for the antitumor activities of new nucleoside antimetabolites, 1-(3- C-ethynyl-β-d-ribo-pentofuranosyl)cytosine and -uracil

We previously designed 1-(3-C-ethynyl-β-D-ribo-pentofuranosyl)uracil (EUrd) and its cytosine congener (ECyd) as potential multifunctional antitumor nucleoside antimetabolites. They showed potent and broad-spectrum antitumor activity against various human

BRANCHED-CHAIN SUGAR NUCLEOSIDES. SYNTHESIS OF 3'-C-ETHYL(AND 3'-C-BUTYL)URIDINE

Syntheses of 3'-C-ethyl(and 3'-C-butyl)uridine (13 and 15) are described.Addition of ethyl (and butyl)magnesium bromide or the corresponding alkyllithiums to 1,2:5,6-di-O-isopropylidene-α-D-ribo-hexofuranos-3-ulose (1) gave 3-C-ethyl (and 3-C-butyl)-1,2:5