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金(I)催化的糖基烯酸酯作为供体的糖苷化反应。

Gold(I)-Catalyzed Glycosylation with Glycosyl Ynenoates as Donors.

机构信息

Shanghai Key Laboratory of New Drug Design, School of Pharmacy , East China University of Science and Technology , 130 Meilong Road , Shanghai 200237 , China.

出版信息

Org Lett. 2019 Dec 6;21(23):9693-9698. doi: 10.1021/acs.orglett.9b03851. Epub 2019 Nov 20.

Abstract

A simple and versatile glycosylation method with both armed and disarmed glycosyl ynenoates as donors is developed. Employing a gold(I) complex as catalyst with or without the assistance of TfOH, the scope of the present glycosylation protocol is very wide. The utility of the present ynenoate donors is demonstrated in the efficient synthesis of oligosaccharides via the latent-active strategy and the multiple orthogonal one-pot strategy. Finally, this approach enables the formal synthesis of the tetrasaccharide hapten of serotype 3 and the highly convergent synthesis of the 32mer polymannoside.

摘要

开发了一种简单且通用的糖基化方法,使用带保护基和去保护基的糖基烯酸酯作为供体。本方法采用金(I)配合物作为催化剂,在有或没有 TfOH 协助的情况下,反应的适用范围非常广泛。烯酸酯供体的应用通过潜伏-活性策略和多种正交一锅法,实现了寡糖的高效合成。最后,该方法还可用于 3 型血清四糖半抗原的形式合成和 32 聚甘露寡糖的高收敛合成。

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