733050-23-2

Upstream product

• 733050-11-8 methyl 3,5-di-O-(4-chlorobenzyl)-2-keto-α-D-ribofuranoside 
• 733050-16-3 2'-α-acetoxymethyl-3',5'-di-O-(4-chlorobenzyl)-2'-deoxyuridine 
• 733050-13-0 methyl 3,5-di-O-(4-chlorobenzyl)-2-deoxy-2-α-(hydroxymethyl)-α-D-ribofuranoside 
• 733050-12-9 methyl-3,5-di-O-(4-chlorobenzyl)-2-deoxy-2-methylene-β-D-ribofuranoside 
• 108008-66-8 methyl 3,5-di-O-(4-chlorobenzyl)-α-D-ribofuranoside 
• 733050-21-0 3',5'-di-O-(4-chlorobenzyl)-2'-deoxy-2'-α-hydroxymethyluridine 
• 733050-14-1 methyl 2α-acetoxymethyl-3,5-di-O-(4-chlorobenzyl)-2-deoxy-α-D-ribofuranoside 

Downstream Products

• 160054-76-2 5'-O-(dimethoxytrityl)-2'-deoxy-2'-α-methyl-N⁴-benzoylcytidine 
• 733050-26-5 3',5'-di-O-(tert-butyldimethylsilyl)-2'-deoxy-2'-α-methyl-N⁴-benzoylcytidine 
• 733050-27-6 2'-deoxy-2'-α-methyl-N⁴-benzoylcytidine 
• 733050-22-1 3',5'-di-O-(4-chlorobenzyl)-2'-deoxy-2'-α-methyluridine 

Relevant academic research and scientific papers

Synthesis of the phosphoramidite derivatives of 2′-deoxy-2′-C- α-methylcytidine and 2′deoxy-2′-C- αhydroxymethylcytidine: Analogues for chemical dissection of RNA's 2′-hydroxyl group

Oligonucleotides containing 2′-C-αmethyl and 2′-C-α-hydroxymethyl modifications enable strategies for delineation of the distinctive role fulfilled by the 2′-hydroxyl group in RNA structure and function. Synthetic routes to the phosphoramidite derivatives