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莪术醇二萜的合成及生物活性

Synthesis and Biological Activities of Scleropentaside D.

机构信息

National Engineering Research Center for Carbohydrate Synthesis, Jiangxi Normal University, Nanchang, 330022, China.

出版信息

J Org Chem. 2024 Jun 21;89(12):9098-9102. doi: 10.1021/acs.joc.4c00755. Epub 2024 Jun 11.

Abstract

We report the first total synthesis of scleropentaside D, a unique -glycosidic ellagitannin, from the ketal derivative of scleropentaside A employing site-selective O4-protection of -acyl glycoside and copper-catalyzed oxidative coupling reaction of galloyl groups as the key steps. Our study confirms the proposed structure of this natural product, scleropentaside D, and demonstrates its effectiveness as an inhibitor of α-glycosidase.

摘要

我们报告了首例 scleropentaside D 的全合成,scleropentaside D 是一种独特的 -糖苷型鞣花单宁,来源于 scleropentaside A 的缩酮衍生物,采用 -酰基糖苷的选择性 O4 保护和邻苯二酚基的铜催化氧化偶联反应为关键步骤。我们的研究证实了这种天然产物 scleropentaside D 的结构,并证明了其作为 α-糖苷酶抑制剂的有效性。

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