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首页> 外文期刊>Bulletin of the Korean Chemical Society >Efficient Synthesis of Novel 4'-TrifluoromethyI-5,-norcarbocycUc Purine Phosphonic Acid Analogs by Using the Ruppert-Prakash Reaction
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Efficient Synthesis of Novel 4'-TrifluoromethyI-5,-norcarbocycUc Purine Phosphonic Acid Analogs by Using the Ruppert-Prakash Reaction

机译:通过Ruppert-Prakash反应有效合成新型4'-三氟甲基I-5,-降碳球菌嘌呤膦酸类似物

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摘要

Novel 4'-trifluoromethyl-5'-norcarbocyclic purine phosphonic acid analogs were efficiently synthesized from commercially available 1,3-dihydroxy cyclopentane (5). Trifluoromethylationwas successfully performed by using the Ruppert-Prakash reaction. The purine nucleosidic bases were efficiently coupled by using the Mitsunobu reaction. The synthesized adenosine phosphonic acids analogs 13 and 16 were screened for antiviral activity against human immunodeficiency virus-1 (HIV-1). Adenine derivative 13 exhibited significant anti-HTV-1 activity.
机译:从市售的1,3-二羟基环戊烷(5)有效合成了新型4'-三氟甲基-5'-降碳环嘌呤膦酸类似物。通过使用Ruppert-Prakash反应成功地进行了三氟甲基化。嘌呤核苷碱基可通过Mitsunobu反应有效地偶联。筛选合成的腺苷膦酸类似物13和16对人免疫缺陷病毒-1(HIV-1)的抗病毒活性。腺嘌呤衍生物13显示出显着的抗HTV-1活性。

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