发明名称 SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDE
摘要 <p>PROBLEM TO BE SOLVED: To provide a method for a solid phase synthesis of an oligonucleotide providing an improved method for removing a protecting group from the oligonucleotide bound to a solid supporting materials. SOLUTION: This method for a solid phase synthesis of an oligonucleotide, is (a) to synthesize nucleic acids consectively on a solid supporting material according to a known method, where amino groups out of ring existing in the nucleic acid base are protected with cyclic diacyl groups, (b) remove a protecting group from the oligonucleotide bound to the solid supporting material by removing a phosphate protecting group with a non-nucleophilic strong base, and (c) separate the protecting group-removed oligonucleotide from the solid supporting material. In this case, the protecting group is removed from the oligonucleotide bound to the solid supporting material by a suitable organic solvent in the presence of the non-nucleophilic strong base.</p>
申请公布号 JPH1072486(A) 申请公布日期 1998.03.17
申请号 JP19970185142 申请日期 1997.07.10
申请人 HOECHST AG 发明人 PFLEIDERER WOLFGANG PROF DR;BEIER MARKUS DIPL CHEM
分类号 C07H19/06;C07F9/6561;C07H19/04;C07H19/16;C07H21/00;(IPC1-7):C07H21/00;C07F9/656 主分类号 C07H19/06
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