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Synthesis of diverse 6-(1,2-disubstituted ethyl)purine bases and nucleosides via 6-(oxiran-2-yl)purines

机译:通过6-(环氧乙烷-2-基)嘌呤合成多种6-(1,2-二取代的乙基)嘌呤碱和核苷

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摘要

Dihydroxylation of 6-vinylpurines with t-BuOOH and OSO4 gave 6-(1,2-dihydroxyethyl)purines 2, while the epoxidation with H2WO4 and t-BuOOH afforded 6-(oxiran-2-yl)purines 3. Oxirane ring-opening reactions of 3 with diverse nucleophiles gave a series of title 6-(1,2-disubstituted ethyl)purine bases and nucleosides, which were tested for cytostatic and antiviral activities. (C) 2008 Published by Elsevier Ltd.
机译:用t-BuOOH和OSO4对6-乙烯基嘌呤进行二羟基化,得到6-(1,2-二羟基乙基)嘌呤2,而用H2WO4和t-BuOOH进行环氧化得到6-(环氧乙烷-2-基)嘌呤3。环氧乙烷开环3与各种亲核试剂的反应给出了一系列标题6-(1,2-二取代的乙基)嘌呤碱基和核苷,并对其细胞抑制和抗病毒活性进行了测试。 (C)2008由Elsevier Ltd.发布

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