70457-82-8Relevant 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
SYNTHESIS OF DEOXYRIBOOLIGONUCLEOTIDES BY USING AROMATIC PHOSPHORAMIDATES AS THE PROTECTING GROUP FOR THE 3'-PHOSPHO ENDS
Ohtsuka, Eiko,Shibahara, Susumu,Ono, Teiichi,Fukui, Toshikazu,Ikehara, Morio
, p. 395 - 398 (2007/10/02)
p-Chlorophenyl phosphoranilidochloridate was used to phosphorylate the 3'-hydroxyl groups of N,5'-O-protected deoxyribonucleotides.These nucleotides served as the 3'-terminal unit in the syntheses of some protected oligonucleotides which were used in a bl
