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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Synthesis of base-modified dihydropacidamycins.
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Synthesis of base-modified dihydropacidamycins.

机译:碱改性二氢丙氨酸的合成。

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摘要

We describe in this paper the synthesis of 1,2-di-O-acetyl-5-azido-3,5-dideoxy-alpha,beta-L-arabinofuranose, a carbohydrate donor that was used for the synthesis of 1-(5'-amino-3',5'-dideoxy-alpha-L-arabinofuranosyl)uracil, the nucleoside found in dihydropacidamycin D. The carbohydrate donor was also used for the synthesis of a set of new nucleosides that were introduced in new dihydropacidamycins. These compounds were tested for biological activity, and the results showed that uracil is the only base recognized by MraY.
机译:我们在本文中描述了1,2-Di-O-乙酰基-5-氮杂-3,5-二赤氧基 - α,β-L-阿拉伯呋喃糖,碳水化合物供体的合成,用于合成1-(5 ' - amino-3',5'-二脱氧-α-L-阿拉伯呋喃糖基)尿嘧啶,二氢丙酰胺蛋白D中发现的核苷。碳水化合物供体也用于合成新的二氢丙氨酸中引入的一组新的核苷。 测试这些化合物的生物活性,结果表明,尿嘧啶是MRAY识别的唯一基地。

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