>Vicinal chloroamines derived from glycals have been converted into the corresponding chiral aziridines. Although the formation of'/> Synthesis of Chiral Aziridines from Glycals: Application in the Synthesis of a Piperidine–Azepine Fused Derivative
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Synthesis of Chiral Aziridines from Glycals: Application in the Synthesis of a Piperidine–Azepine Fused Derivative

机译:来自血糖的手性阿氮吡啶的合成:应用在哌啶 - 哌齐融合衍生物的合成中

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摘要

>Vicinal chloroamines derived from glycals have been converted into the corresponding chiral aziridines. Although the formation of a tetrahydrofuran derivative is also possible, reaction conditions were developed to give the azirdines exclusively. One of the aziridines is closely related to a compound used in the synthesis of an advanced intermediate en route to Zanamivir, an antiviral agent. Furthermore, one of the aziridines was converted into a piperidine–azepine fused derivative.
机译: >源自族种的邻近氯胺已被转换为相应的手性阿齐西语。 尽管也可以形成四氢呋喃衍生物,但是开发了反应条件以专门给予氮氧态。 其中一种氮化物与用于合成到Zanamivir的先进中间体,抗病毒剂的化合物密切相关。 此外,将其中一种氮化物转化为哌啶 - 偶氮融合衍生物。

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