98264-12-1

Upstream product

• 81243-97-2 2'-O-tetrahydropyranyl-5',3'-O-(tetraisopropyldisiloxane-1,3-diyl)uridine 
• 100-07-2 4-methoxy-benzoyl chloride 
• 69304-38-7 3',5'-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)uridine 
• 119694-66-5 4-O-<(2,4,6-triisopropylphenyl)sulfonyl>-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)uridine 

Downstream Products

• 98889-30-6 N³-anisoyl-2'-O-(tetrahydropyran-2-yl)-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)uridine 
• 86964-78-5 S,S-diphenyl 2'-O-(tetrahydropyran-2-yl)-5'-O-(4,4'-dimethoxytrityl)-N³-anisoyluridine-3'-phosphorodithioate 
• 86964-81-0 S,S-diphenyl 2'-O-(tetrahydropyran-2-yl)-N³-anisoyl-uridine 3'phosphorodithioate 
• 98889-31-7 N³-anisoyl-2'-O-(tetrahydropyran-2-yl)-5'-O-dimethoxytrityluridine 

Relevant academic research and scientific papers

General Method for the Preparation of N3- and O4-Substituted Uridine Derivatives by Phase-Transfer Reactions

A general method for regioselective introduction of a variety of protecting groups into the uracil residue of 1 has been developed by use of the phase-transfer reaction.Under such conditions, acyl groups such as benzoyl, p-toluyl, p-anisoyl, (2,2,2-trichl

Chemical Synthesis of Capped Oligoribonucleotides, m7G5'pppAUG and m7G5'pppAUGACC

The fully-protected pAUG(15) and pAUGACC(21) were synthesized by the phosphotriester approach where the phenylthio group was employed as the internal and 5'-terminal phosphate-protecting groups.The partially unblocked oligomers (32) and (33), obtained by