727416-05-9

Upstream product

• 182687-79-2 1-[2,3,6-tri-O-acetyl-4-deoxy-4-C-hydroxymethyl-α-L-lyxopyranosyl]thymine 
• 182687-70-3 2,3,6-tri-O-acetyl-4-deoxy-4-C-hydroxymethyl-1-O-methyl-α-L-lyxopyranose 
• 182687-68-9 4-deoxy-4-C-hydroxymethyl-2,3-O-isopropylidene-1-O-methyl-α-L-lyxopyranose 
• 182687-64-5 1-[4-deoxy-4-C-hydroxymethyl-α-L-lyxopyranosyl]thymine 
• 65-71-4 thymin 
• 2495-99-0 methyl 2,3-O-isopropylidene-α-L-lyxopyranoside 
• 182687-88-3 4-deoxy-4-C-hydroxymethyl-1-O-methyl-α-L-lyxopyranose 
• 1005-56-7 phenylcarbonochloridothioate 
• 727416-04-8 1-[4-deoxy-4-C-hydroxymethyl-3,6-O-(1,1,3,3-tetraisopropyldisiloxan-1,3-diyl)-α-L-lyxopyranosyl]thymine 
• 727416-02-6 2,3-O-isopropylidene-1-O-methyl-4-O-phenoxythiocarbonyl-α-L-lyxopyranose 
• 727416-03-7 2,3-O-isopropylidene-1-O-methyl-4-C-(2-phenylethenyl)-α-L-lyxopyranose 
• 7288-28-0 2,4-bis(trimethylsiloxy)-5-methylpyrimidine 

Relevant academic research and scientific papers

Synthesis and conformational analysis of 1-[2,4-dideoxy-4-C-hydroxymethyl- α-L-lyxopyranosyl]thymine

Previously different types of nucleosides with a six-membered carbohydrate moiety have been evaluated for their potential antiviral and antibiotic properties and as building blocks in nucleic acid synthesis. However, a pyranose nucleoside with a 1,4-subst