89947-90-0

Upstream product

• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 51549-30-5 5'-O-(tert-butyldimethylsilyl)-2'-deoxyadenosine 
• 89947-89-7 5'-O-t-butyldimethylsilyl-N,3'-O-bis(di-p-methoxytrityl) deoxyadenosine 

Downstream Products

• 222171-13-3 N-{9-[4-hydroxy-5-([2,2';6',2'']terpyridin-4'-yloxymethyl)-tetrahydro-furan-2-yl]-9H-purin-6-yl}-benzamide 
• 222171-10-0 {9-[(2R,4S,5R)-4-[Bis-(4-methoxy-phenyl)-phenyl-methoxy]-5-([2,2';6',2'']terpyridin-4'-yloxymethyl)-tetrahydro-furan-2-yl]-9H-purin-6-yl}-[bis-(4-methoxy-phenyl)-phenyl-methyl]-amine 

Relevant academic research and scientific papers

Efficient site-specific cleavage of RNA using a terpyridine-copper(II) complex joined to a 2'-O-methyloligonucleotide by a non-flexible linker

A terpyridine-Cu(II) complex conjugated to an antisense 2'O-methyloligonucleotide at the 5'-end cleaved RNA predominantly at the site opposite the 5'-end in moderate yield, but the cleavage yield increased by more than two-fold when a 2'-O-methyloligonucl

Site-specific RNA cleavage using terpyridine · Cu(II)-linked 2'-O- methyloligonucleotides

2'-Deoxy- and 2'-O-methyl-5'-O-terpyridyl derivatives of adenosine and cytidine were synthesized and used to construct 5'-end-modified oligonucleotides. These antisense agents complexed with Cu(II) exclusively cleaved a complementary RNA oligomer at the s

STEREOSPECIFIC SYNTHESIS OF DINUCLEOSIDE MONOPHOSPHATE ARYL ESTERS BY USING NEW CONDENSING REAGENTS

New condensing reagents, arenesulfonyl 5-(pyridin-2-yl)tetrazoles have been synthesized and used for stereospecific synthesis of dinucleoside monophosphate aryl esters.