Centre for Synthesis and Chemical Biology, UCD School of Chemistry, University College Dublin, Belfield, Dublin 4, Ireland.
Org Biomol Chem. 2019 Aug 28;17(32):7531-7535. doi: 10.1039/c9ob01544b. Epub 2019 Aug 1.
The stereoselective synthesis of glycosyl chlorides using catalytic Appel conditions is described. Good yields of α-glycosyl chlorides were obtained using a range of glycosyl hemiacetals, oxalyl chloride and 5 mol% PhPO. For 2-deoxysugars treatment of the corresponding hemiacetals with oxalyl chloride without phosphine oxide catalyst also gave good yields of glycosyl chloride. The method is operationaly simple and the 5 mol% phosphine oxide by-product can be removed easily. Alternatively a one-pot, multi-catalyst glycosylation can be carried out to transform the glycosyl hemiacetal directly to a glycoside.
本文描述了使用催化 Appel 条件立体选择性合成糖苷氯的方法。使用一系列糖基半缩醛、草酰氯和 5 mol% PhPO,可获得α-糖苷氯的良好产率。对于 2-脱氧糖,未经膦氧化物催化剂处理相应的半缩醛也可得到糖苷氯的良好产率。该方法操作简单,可轻松去除 5 mol%的氧化膦副产物。或者,可以进行一锅多催化剂糖基化反应,将糖基半缩醛直接转化为糖苷。