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A Facile Synthesis of Anomeric Benzyl Protected Man-Β(1,4)GlcNAc Scaffold as a Building Block for a Rapid Expansion of Oligosaccharide Molecular Diversity 异头苯基保护Man-Β(1,4)GlcNAc支架的简易合成:快速扩展寡糖分子多样性的构建块
Pub Date : 1900-01-01 DOI: 10.2139/ssrn.3903182
J. I. Ayogu
A facile and efficient strategy for accessing Man-β(1,4)GlcNAc core was investigated. Anomeric benzyl protected acceptor derived from N-glycosamine hydrochloride was glycosylated with orthogonally protected thioglycoside to afford the gluc-β(1,4)GlcNAc scaffold which was epimerized via triflation to obtain the Man-β(1,4)GlcNAc derivative. The disaccharide Man-β(1,4)GlcNAc scaffold could be used as the basic building block for the divergent synthesis of various oligosaccharide structures for detailed biological activity investigation of glycans. The compounds were characterized by NMR, MS and Infra-red (IR) spectroscopy.
研究了一种简单有效的获取Man-β(1,4)GlcNAc核心的方法。从n-氨基糖胺盐酸盐中得到的异头苯基保护受体与正交保护的巯基糖苷进行糖基化,得到葡萄糖-β(1,4)GlcNAc支架,经三倍压外聚得到Man-β(1,4)GlcNAc衍生物。双糖Man-β(1,4)GlcNAc支架可作为各种低聚糖结构的发散合成的基本构建块,用于详细的多糖生物活性研究。通过核磁共振、质谱和红外光谱对化合物进行了表征。
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ChemRN: Natural Product Chemistry (Topic)
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