首页> 外文期刊>European journal of organic chemistry >A Strategy for the Stereoselective Preparation of Thymidine Phosphorothioates with the (R)or the (S)Configuration at the Stereogenic Phosphorus Atom and Their Application to the Synthesis of Oligodeoxyribonucleotides with Stereochemically Pure Phosph
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A Strategy for the Stereoselective Preparation of Thymidine Phosphorothioates with the (R)or the (S)Configuration at the Stereogenic Phosphorus Atom and Their Application to the Synthesis of Oligodeoxyribonucleotides with Stereochemically Pure Phosph

机译:立体生成磷原子上具有(R)或(S)构型的胸腺嘧啶硫代磷酸酯的立体选择性制备策略及其在立体化学纯磷酸合成寡聚脱氧核糖核苷酸中的应用

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This paper describes a new method for the highly stereoselective preparation of dithymidine phosphorothioates (TpsT)with the (R)or the (S)configuration at the stereogenic phosphorus atom [(Rp)-or (Sp)-TpsT,respectively],together with the synthesis of oligodeoxyribonucleotides with stereochemically pure phosphate/phosphorothioate mixed backbones through the use of (Rp)-or (Sp)-TpsT as building blocks.Stereochemically pure (Rp)-or (Sp)-TpsT was produced through a five-step process:1)lH-tetrazole-promoted thermodynamic equilibration of a diastereomeric mixture of allyl (Rp)-and (Sp)-thymidine 3',5'-cyclic phosphate to give the (Sp)isomer as the major component,2)stereospecific sul-furization of the allyl (Sp)-thymidine 3',5'-cyclic phosphate to afford an allyl (Rp)-thymidine 3',5'-cyclic phosphorothioate,3)regioselective and stereoselective methanolysis of the allyl (Rp)-thymidine 3',5'-cyclic phosphorothioate to provide an allyl methyl (Rp)-thymidine 3'-phosphorothioate as the main product,4)stereospecific removal of the methyl group from the phosphorothioate moiety to give an allyl (Rp)-5'-O-di-methoxytritylthymidine 3'-phosphorothioate diester,or stereospecific removal of the allyl group from the phosphate moiety to form a methyl (Sp)-5'-O-dimethoxytritylthymidine 3'-phosphorothioate diester,and 5)stereospecific condensation of these (Rp)-and (Sp)-diesters with a 5'-O-free thymidine in a Mitsunobu reaction to produce the allyl (3'-5')-linked (Sp)-dithymidine phosphorothioate and the methyl (3'-5')-linked (Rp)-dithymidine phosphorothioate,respectively.The resulting (Rp)-and (Sp)-dithymidine phosphorothioates were converted into their 3'-phosphoramidites.Oligodeoxyribonucleotides with stereochemically pure phosphate/phos-phorothioate-mixed backbones were then synthesized by use of these phosphoramidites as building blocks.
机译:本文描述了一种新的方法,该方法可在立体磷原子[分别为(Rp)-或(Sp)-TpsT]处具有(R)或(S)构型的高立体选择性制备硫代磷酸二胸苷(TpsT)以及通过使用(Rp)-或(Sp)-TpsT作为结构单元,合成具有立体化学纯的磷酸盐/硫代磷酸酯混合骨架的寡脱氧核糖核苷酸。通过五步法生产立体化学纯的(Rp)-或(Sp)-TpsT :1)1H-四唑促进烯丙基(Rp)-和(Sp)-胸苷3',5'-环磷酸的非对映异构体混合物的热力学平衡,得到(Sp)异构体为主要成分,2)立体特异性磺基-精制烯丙基(Sp)-胸苷3',5'-环磷酸酯,得到烯丙基(Rp)-胸苷3',5'-环硫代磷酸酯,3)烯丙基(Rp)-胸苷的区域选择性和立体选择性甲醇分解3',5'-环硫代磷酸酯可提供烯丙基甲基(Rp)-胸苷3'-硫代磷酸酯作为主要产品ct,4)从硫代磷酸酯部分中立体选择性除去甲基,得到烯丙基(Rp)-5'-O-二甲氧基三苯甲基胸苷3'-硫代磷酸酯二酯,或从磷酸酯部分中立体定向去除烯丙基以形成α (Sp)-5'-O-二甲氧基三苯甲基三甲基胸苷3'-硫代磷酸二酯,以及这些(Rp)-和(Sp)-二酯与5'-O-无胸腺嘧啶的5)立体特异性缩合,以产生Mitsunobu反应烯丙基(3'-5')-连接的(Sp)-二胸苷硫代磷酸酯和甲基(3'-5')-连接的(Rp)-二胸苷硫代磷酸酯,生成的(Rp)-和(Sp)-二胸苷硫代磷酸酯然后用这些亚磷酰胺作为结构单元合成具有立体化学纯的磷酸盐/磷-硫代磷酸酯主链的低聚脱氧核糖核苷酸。

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