144944-91-2

Upstream product

• 3444-09-5 1,3-bis(trimethylsilyl)thymine 
• 144944-83-2 3-deoxy-3-C-(2'-hydroxyethyl)-1,2-O-isopropylidene-2'-O-para-methoxyphenyl-5-O-trityl-α-D-ribofuranose 
• 144944-85-4 2',5'-di-O-acetyl-3'-deoxy-3'-C-(2-hydroxyethyl)-2-O-para-methoxyphenyl-(β-D-ribofuranosyl)thymine 
• 144944-84-3 1,2,5-tri-O-acetyl-3-deoxy-3-C-(2'-hydroxyethyl)-2'-O-para-methoxyphenyl-β-D-ribofuranose 
• 150-76-5 4-methoxy-phenol 
• 58399-76-1 3-Deoxy-3-C-(2'-hydroxyethyl)-1,2-O-isopropylidene-5-O-(triphenylmethyl)-α-D-ribofuranose 
• 144944-86-5 3'-deoxy-3'-C-(2-hydroxyethyl)-2-O-para-methoxyphenyl-(β-D-ribofuranosyl)thymine 
• 507-09-5 tiolacetic acid 

Downstream Products

• 144944-90-1 3',5'-dideoxy-3'-C-(2-hydroxyethyl)-2-O-para-methoxyphenyl-5'-thiothymidine 
• 144944-92-3 5'-S-acetyl-3',5'-dideoxy-3'-C-(2-hydroxyethyl)-2-O-para-methoxyphenyl-5'-thiothymidine 

Relevant academic research and scientific papers

Synthesis of thymidine building blocks for a nonhydrolyzable DNA analogue

The 3'-deoxy-3'-C-(2"-hydroxyethyl)thymidine derivatives 4 and 13 were efficiently synthesized from either thymidine via a known 3'-radical allylation, or from the branched-chain furanose 5 involving the removal of the 2'-hydroxyl after stereospecific nuc