摘要 |
A method for preparing an oligonucleotide comprising the steps of a) providing a 3'-protected compound having the formula: <CHEM> wherein B is a heterocyclic base R2 is H, a protected 2'-hydroxyl group, F, a protected amino group, an O-alkyl group, an O-substituted alkyl, a substituted alkylamino or a C4'-O2'methylen linkage R3 is a hydroxyl protecting group, a 3'-protected nucleotide or a 3'-protected oligonucleotide b) reacting said compound with a nucleotide derivative having a 5'-proctection group in the presence of a solid supported activator to give an elongated oligonucleotide with a P(III)-internucleotide bond c) processing the elongated oligonucleotide with a P(III)-internucleotide bond by steps c1) and c2) in any sequence c1) capping by reacting with a solid supported capping agent c2) oxidizing by reacting the oligonucleotide with a solid supported oxidizing reagent d) removing the 5'-protection group by treatment with a solid supported agent or removing the 5'-protection group with a removal agent followed by addition of a solid supported scavenger or followed by extraction. |
申请人 |
GIRINDUS AG;CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE - CNRS;L'UNIVERSITE MONTPELLIER II |
发明人 |
ADAMO, ILARIA;DUEYMES, CECILE;SCHOENBERGER, ANDREAS;IMBACH, JEAN-LOUIS;MEYER, ALBERT;MORVAN, FRANCOIS;DEBART, FRANCOISE;VASSEUR, JEAN-JACQUES;LANGE, MEINOLF;LINK, FRITZ |