84774-19-6Relevant academic research and scientific papers
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
THE CHEMICAL SYNTHESIS OF THE Rp AND Sp DIASTEREOMERS OF THYMIDYL-(3'-5')THYMIDYL O,O-PHOSPHOROTHIOATE
Uznanski, Bogdan,Niewiarowski, Wojciech,Stec, Wojciech J.
, p. 4289 - 4292 (2007/10/02)
The synthesis and separation of diastereomers of protected thymidyl-(3'-5')thymidyl O,O-phosphoranilidate (4) allowed to obtain in the stereospecific manner title compounds 5, whose absulute configuration at P atom was assigned enzymatically.TP(S)T diastereomers (5) were obtained independently via "phosphite" procedure.
