213548-82-4

Upstream product

• 120402-66-6 4-Methoxytrityl 4-hydroxybenzyl ether 
• 623-05-2 (4-hydroxyphenyl)methanol 
• 213548-43-7 2'-O-{1-{{4-{{[2-(4-nitrophenyl)ethoxy]carbonyl}oxy}benzyl}oxy}ethyl}-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)uridine 
• 213547-92-3 4-[2-(4-Nitrophenyl)ethoxycarbonyloxy]benzyl vinyl ether 
• 213549-10-1 4[2-(4-Nitrophenyl)ethoxycarbonyloxy]benzyl alcohol 

Downstream Products

• 356065-77-5 5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-O-{1-{{4-{{[2-(4-nitrophenyl)ethoxy]carbonyl}oxy}benzyl}oxy}ethyl}uridine 

Relevant academic research and scientific papers

Nucleotides. Part LXVIII. Acetals as New 2'-O-Protecting Functions for the Synthesis of Oligoribonucleotides: Synthesis of Monomeric Building Units and Oligoribonucleotides

For the efficient synthesis of oligoribonucleotides by the 5'-O-(4,4'-dimethoxytrityl) phosphoramidite approach, the 2'-O-[1-(benzyloxy)ethyl]acetals 56-67 were investigated. Studies with the 2'-O-[1-(benzyloxy)ethyl]-5'-O-(dimethoxytrityl)ribonucleoside

Acetals as New 2′-O-Protecting Functions for the Synthesis of Oligoribonucleotides: Synthesis of Uridine Building Blocks and Evaluation of Their Relative Acid Stability

A broad variety of new acyclic vinyl ethers (see 6-41) have been synthesized via the vinyl-interchange reaction of ethyl vinyl ether at room temperature using mercury(II) trifluoroacetate as a highly efficient catalyst. The appropriate vinyl ethers were r

Solid-phase synthesis of oligoribonucleotides

A process for the preparation of oligoribonucleotides of the formula STR1 in which n, L, BB, W, T, Y', U, C1 and C2 are as defined in the description, by solid-phase synthesis is described, as are intermediates of the oligoribonucleo