STEREOSELECTIVE GLYCOSYLATION OF ALCOHOLS AND SILYL ETHERS USING GLYCOSYL FLUORIDES AND BORON-TRIFLUORIDE ETHERATE
STEREOSELECTIVE GLYCOSYLATION OF ALCOHOLS AND SILYL ETHERS USING GLYCOSYL FLUORIDES AND BORON-TRIFLUORIDE ETHERATE
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DOI：
10.1002/hlca.19850680134
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发表时间：
1985-01-01
影响因子：
1.8
通讯作者：
SAGER, W
中科院分区：
文献类型：
--
作者：
KUNZ, H;SAGER, W
醇及其甲硅烷基醚的立体选择性糖基化已经使用吡喃糖和呋喃糖系列的O-烷基-、O-酰基-和缩醛保护的糖基氟化物以及三氟化硼醚合物在CH 2Cl 2中实现。
The stereoselective glycosylation of alcohols and their silyl ethers has been achieved using O-alkyl-, O-acyl-, and acetal-protected glycosyl fluorides of the pyranose and furanose series, and boron trifluoride etherate in CH2Cl2.