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使用催化 Appel 条件合成糖基氯化物。

Synthesis of glycosyl chlorides using catalytic Appel conditions.

机构信息

Centre for Synthesis and Chemical Biology, UCD School of Chemistry, University College Dublin, Belfield, Dublin 4, Ireland.

出版信息

Org Biomol Chem. 2019 Aug 28;17(32):7531-7535. doi: 10.1039/c9ob01544b. Epub 2019 Aug 1.

Abstract

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.

摘要

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。

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