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首页> 外文期刊>Nucleosides, nucleotides and nucleic acids >SYNTHESIS AND POTENT ANTI-LEUKEMIC ACTIVITY OF NOVEL 5 '-DEOXYCARBOCYCLIC C-NUCLEOSIDE PHOSPHONIC ACIDS
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SYNTHESIS AND POTENT ANTI-LEUKEMIC ACTIVITY OF NOVEL 5 '-DEOXYCARBOCYCLIC C-NUCLEOSIDE PHOSPHONIC ACIDS

机译:5'-脱氧碳环C-核苷磷酸的合成及潜在的抗白血病活性

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摘要

The first synthetic route to 5-deoxycarbocyclic C-nucleoside [9-deazaadenosine, (pyrrolo[3,2-d]pyrimidine)] phosphonic acids from commercially available 1,4-dihydroxy-2-butene was described. The key C-C bond formation from cyclopentanone to base precursor was performed using Knoevenagel-type condensation. Synthesized C-nucleoside phosphonic acids were tested for anti-HIV activity as well as anti-leukemic activity. They showed moderate cytotoxicity derived anti-HIV activity and anti-leukemic activity.
机译:描述了从可商购的1,4-二羟基-2-丁烯到5-脱氧碳环C-核苷[9-脱氮杂腺苷,(吡咯并[3,2-d]嘧啶)]膦酸的第一合成路线。从环戊酮到基础前体的关键C-C键形成是使用Knoevenagel型缩合进行的。测试了合成的C-核苷膦酸的抗HIV活性以及抗白血病活性。他们显示出中等的细胞毒性衍生的抗HIV活性和抗白血病活性。

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