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新型隐球菌 B 型荚膜重复基元的会聚全合成。

Convergent total synthesis of Cryptococcus neoformans serotype B capsule repeating motif.

机构信息

Centre for Synthesis and Chemical Biology, University College Dublin, Belfield, Dublin, Ireland.

Centre for Synthesis and Chemical Biology, University College Dublin, Belfield, Dublin, Ireland.

出版信息

Carbohydr Res. 2020 Nov;497:108150. doi: 10.1016/j.carres.2020.108150. Epub 2020 Sep 7.

Abstract

Cryptococcus neoformans is an opportunistic fungal pathogen, which is a frequent cause of a life-threatening meningitis in immunocompromised individuals. We report the first total synthesis of the serotype B heptasaccharide repeating motif. The use of di- and trisaccharide building blocks enabled a concise convergent synthesis of the protected 6-O-acetylated repeating motif in three steps. Glycosylations gave total 1,2-trans selectivity, despite the absence of a neighboring participating group. Using our recently disclosed catalyst pre-tuning strategy global deprotection gave the desired 6-O-acetylated heptasaccharide with no saturation by-products, overall in four steps 31% yield. The serotype B glucuronoxylomannan (GXM) glycans accessed in this study will increase the structurally diversity of our GXM microarray, allowing further steps towards the development of semi-synthetic vaccines against cryptococcal infections.

摘要

新型隐球菌是一种机会性真菌病原体,是免疫功能低下个体中一种危及生命的脑膜炎的常见病因。我们报告了血清型 B 七糖重复基元的首次全合成。使用二糖和三糖砌块能够以三步实现保护的 6-O-乙酰化重复基元的简洁收敛合成。尽管没有相邻的参与基团,但糖基化仍具有总 1,2-反式选择性。使用我们最近公开的催化剂预调谐策略进行全局脱保护,得到了所需的 6-O-乙酰化七糖,没有饱和副产物,总收率为 4 步 31%。本研究中获得的血清型 B 葡糖醛酸甘露聚糖(GXM)聚糖将增加我们 GXM 微阵列的结构多样性,从而进一步开发针对隐球菌感染的半合成疫苗。

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