153413-69-5Relevant academic research and scientific papers
Studies on oxidative transformations of dinucleoside H-phosphonoselenoates
Bollmark, Martin,Kullberg, Martin,Stawinski, Jacek
, p. 832 - 841 (2006)
The utility of a new type of synthetic intermediates, H-phosphonoselenoate diesters, in the preparation of potentially biologically important nucleotide analogues containing the P-Se bond, was explored by converting dinucleoside H-phosphonoselenoates 1 in
New phosphitylating reagent in the nucleotide chemistry containing two 4-nitrophenoxy leaving groups. Remarkably fast and clean phosphitylations activated by DBU leading to thio- and seleno-oligonucleotides
Helinski, Jan,Dabkowski, Wojciech,Michalski, Jan
, p. 6451 - 6454 (2007/10/02)
A new synthetic approach to modified oligonucleotides based on N,N′-diisopropyl-di-(4-nitrophenyl)phosphoroamidite 1 is described. The procedure involves displacement of either 4-nitrophenoxy or diisopropylamino ligands. The former proceeds very fast in t
