首页> 外国专利> OPTICALLY ACTIVE SEGMENT FOR USE IN SYNTHESIS OF STEREOCONTROLLED OLIGONUCLEOTIDE, METHOD FOR PRODUCING THE SAME, AND METHOD FOR SYNTHESIZING STEREOCONTROLLED OLIGONUCLEOTIDE USING THE SAME

OPTICALLY ACTIVE SEGMENT FOR USE IN SYNTHESIS OF STEREOCONTROLLED OLIGONUCLEOTIDE, METHOD FOR PRODUCING THE SAME, AND METHOD FOR SYNTHESIZING STEREOCONTROLLED OLIGONUCLEOTIDE USING THE SAME

机译:用于合成立体控制的寡核苷酸的光学活性段,制备方法,以及使用该制备方法的制备方法,以及合成立体控制寡核苷酸的方法

摘要

An optically active segment for use in synthesis of a stereocontrolled oligonucleotide represented by the following formula (I), a method for producing the same, and a method for synthesizing a stereocontrolled oligonucleotide therefrom are provided. In formula, B is a protected/unprotected nucleoside base; R1 is substituted/unsubstituted aliphatic group; R2, R3 is a DMTr group or —P(R11)(NR12)2; R11 is OCH2CH2CN, SCH2CH2CN, etc.; R12 is a substituted/unsubstituted aliphatic group or aromatic group; X is H, an alkyl, O-alkyl, etc.; Y is H, NHR13, a halogen, etc., or a hydroxyl group protected with an acyl, ether, or silyl, or forms an X—Y bond with X; and n is an integer of 0 or more and 4 or less.;
机译:提供用于合成由下式(I)表示的立体控制寡核苷酸的光学活性段,其制备方法,以及用于合成其上的立体控制寡核苷酸的方法。 在式中,B是受保护/未受保护的核苷基础; R1是取代/未取代的脂肪族基团; R2,R3是DMTR组或-P(R11)(NR12)2; R11是OCH2CH2CN,SCH2CH2CN等; R12是取代/未取代的脂族基团或芳族基团; X是H,烷基,O-烷基等; Y是H,NHR13,卤素等,或用酰基,醚或甲硅烷基保护的羟基,或与X形成X-Y键; n是0或更多,4或更小的整数;

著录项

  • 公开/公告号US2021317158A1

    专利类型

  • 公开/公告日2021-10-14

    原文格式PDF

  • 申请/专利权人 NATIAS INC.;

    申请/专利号US201917051936

  • 发明设计人 MASANORI KATAOKA;MAMORU HYODO;

    申请日2019-05-07

  • 分类号C07H21/04;C07H1/02;

  • 国家 US

  • 入库时间 2022-08-24 21:40:52

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