289486-00-6

Upstream product

• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 167629-46-1 (p-methoxybenzyloxy)-2-hydroxybutanol 
• 167629-45-0 4-[2-(4-methoxy-benzyloxy)ethyl]-2,2-dimethyl-[1,3]dioxolane 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 289486-03-9 1-(4,4'-dimethoxytrityloxy)-4-(p-methoxybenzyloxy)-2-methylenebutane 
• 1026475-63-7 1-{2-[2-(4-methoxy-benzyloxy)-ethyl]-allyl}-5-methyl-1H-pyrimidine-2,4-dione 
• 167629-40-5 4-[(4-methoxybenzyl)oxy]-2-methylenebutan-1-ol 
• 289486-02-8 1-(4,4'-dimethoxytrityloxy)-4-(p-methoxybenzyloxy)butan-2-one 

Relevant academic research and scientific papers

Synthesis of unsaturated carboacyclic nucleoside analogues via Mitsunobu reactions

2-Substituted allyl alcohols 9 and 14 were prepared starting from butane-1,2,4-triol and glycerol, respectively. Mitsunobu condensations of 9 and 14 with purine and pyrimidine bases, followed by deprotection, afforded a number of acyclonucleosides having