Centre for Synthesis and Chemical Biology, University College Dublin, Belfield, Dublin, Ireland.
Centre for Synthesis and Chemical Biology, University College Dublin, Belfield, Dublin, Ireland.
Carbohydr Res. 2020 Nov;497:108150. doi: 10.1016/j.carres.2020.108150. Epub 2020 Sep 7.
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.
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。