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DIASTEREOSELECTIVE SYNTHESIS METHOD OF OPTICALLY ACTIVE CIS-NUCLEOSIDES, THEIR ANALOGS AND DERIVATIVES, AS WELL AS INTERMEDIATES EMPLOYED IN THE PROPOSED METHOD
DIASTEREOSELECTIVE SYNTHESIS METHOD OF OPTICALLY ACTIVE CIS-NUCLEOSIDES, THEIR ANALOGS AND DERIVATIVES, AS WELL AS INTERMEDIATES EMPLOYED IN THE PROPOSED METHOD
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机译:光学活性CIS-核的非对映选择性合成方法,其类似物和衍生物以及所提议方法中使用的中间体
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摘要
A process for the diastereoselective synthesis of optically active cis nucleosides and analogs and derivatives thereof of formula (I), wherein W is O, S, S, S, S, S or methylene; X is O, S, sulfinyl, sulfonyl, NZ, methylene or CHF, CH, CHN3 or CHOH; Y is O, S, CH3 or CH, CHF or CHOH; Z is hydrogen, hydroxy, alkyl, or acyl; R.sub.1 represents a hydrogen atom or an acyl group; and R.sub.2 represents a residue of the desired purine or pyrimidine base or an analogue or derivative thereof; wherein when Y is methylene and X is O, S, S or S, W is not O, S, S or S, by glycosylation of the desired purine or
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机译:式(I)的光学活性顺式核苷及其类似物和衍生物的非对映选择性合成方法,其中W为O,S,S,S,S,S,S或亚甲基; X是O,S,亚磺酰基,磺酰基,NZ,亚甲基或CHF,CH,CHN 3或CHOH; Y为O,S,CH 3或CH,CHF或CHOH; Z为氢,羟基,烷基或酰基; R 1代表氢原子或酰基; R 2代表所需的嘌呤或嘧啶碱基或其类似物或衍生物的残基;其中当Y是亚甲基并且X是O,S,S或S时,W不是O,S,S或S,通过所需嘌呤的糖基化或
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