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通过保护基操作从端基羟化物立体选择性合成糖基叠氮化物。

Stereoselective synthesis of glycosyl azides from anomeric hydroxides via protecting group manipulations.

机构信息

Department of Chemistry & Chemical Biology, Indian Institute of Technology (ISM) Dhanbad, Dhanbad, 826004, Jharkhand, India.

Department of Chemistry & Chemical Biology, Indian Institute of Technology (ISM) Dhanbad, Dhanbad, 826004, Jharkhand, India.

出版信息

Carbohydr Res. 2023 Jan;523:108739. doi: 10.1016/j.carres.2023.108739. Epub 2023 Jan 9.

Abstract

Herein, we report the direct conversion of anomeric hydroxides to glycosyl azides in one step using diphenylphosphoryl azide. Protecting group manipulations on the hexose sugars have enabled the stereoselective synthesis of either the α-glycosyl azides or the β-anomeric azides in moderate to very good yields. The reaction has also been successfully used to enable the synthesis of β-2-deoxy-2-aminoglucosyl azides.

摘要

在此,我们报告了使用二苯磷酰基叠氮化物一步将糖苷羟基转化为糖苷叠氮化物。在己糖糖上进行保护基操作,使得能够以中等至非常好的产率立体选择性地合成α-糖苷叠氮化物或β-端基叠氮化物。该反应还成功地用于合成β-2-脱氧-2-氨基葡萄糖基叠氮化物。

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