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The Synthesis of an Antiviral Fluorinated Purine Nucleoside: 3'-α-Fluoro-2',3'-dideoxyguanosine

机译:抗病毒氟化嘌呤核苷的合成:3'-α-氟-2',3'-二脱氧鸟苷

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摘要

In this review, the synthesis of FddG, a potential HIV reverse transcriptase inhibitor is described focusing on regio- and stereoselective fluorination at the C3'α-position of the nucleoside. These results, which include a synthetic strategy employing retentive fluorination, may provide a new approach towards a variety of C3'α -substituted nucleosides.
机译:在这篇综述中,描述了潜在的HIV逆转录酶抑制剂FddG的合成,着重于核苷C3'α位的区域和立体选择性氟化。这些结果,包括采用保持性氟化的合成策略,可以提供针对各种C3'α-取代核苷的新方法。

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