69330-95-6Relevant academic research and scientific papers
Ribonucleoside Cyclic 3',5'-Phosphoramidates: Synthesis, Stereochemistry, and Conversion into Ribonucleoside Cyclic 3',5'-Phosphorothioates and -Phosphates
Baraniak, Janina,Stec, Wojcieh J.
, p. 1645 - 1656 (2007/10/02)
Base- and O2'-protected nucleoside cyclic 3',5'-phosphates (1) react with aniline in the presence of triphenylphosphine-carbon tetrachloride to give the nucleoside cyclic 3',5'-phosphoramidates (2), which after separation into individual diaste
2'-DEOXYRIBONUCLEOSIDE 3'-ARYL PHOSPHORANILIDATES KEY INTERMEDIATES IN THE STEREOSPECIFIC SYNTHESIS OF 2'-DEOXYRIBONUCLEOSIDE CYCLIC 3',5'-PHOSPHOROTHIOATES AND DINUCLEOSIDE(3'->5')-PHOSPHOROTHIOATES
Lesnikowski, Z. J.,Niewiarowski, W.,Zielinski, W. S.,Stec, W. J.
, p. 15 - 32 (2007/10/02)
Phosphorylation of the 5'-O-monomethoxytrityl-2'-deoxyribonucleosides by means of aryl phosphoranilidochloridates gives the diastereomers of 5'-O-monomethoxytrityl-2'-deoxyribonucleoside 3'-aryl phosphoranilidates.Their separation can be performed by mean
