Synthesis of Glycosides with 4-(4-Hydroxyphenyl)-1,2,3-thia- and -selenadiazole Aglycones

被引:0
作者
L. M. Pevzner
M. L. Petrov
E. B. Erkhitueva
V. A. Polukeev
A. V. Stepakov
机构
[1] St. Petersburg State Institute of Technology (Technical University),
[2] St. Petersburg State University,undefined
[3] Institute of Experimental Medicine,undefined
来源
Russian Journal of General Chemistry | 2019年 / 89卷
关键词
glycosylation; Könnigs-Knorr reaction; interphase catalysis; 1,2,3-thiadiazoles; semicarbazides; 1,2,3-selenadiazoles;
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学科分类号
摘要
Glycosylation of 4-(4-hydroxyphenyl)-1,2,3-thia(selena)diazoles with 1-α-bromo-2,3,4,6-tetra-O-acetyl-D-glucopyranose, 1-α-bromo-2,3,4,6-tetra-O-acetyl-D-galactopyranose, and 1-α-bromo-2,3,5-tri-O-acetyl-D-xylopyranose under the conditions of interphase catalysis has afforded the corresponding acetylated glycosides. An alternative pathway of selenadiasole glycosides synthesis from semicarbazones of 1-β-O-(4-acetylphenyl)-2,3,4,6-tetra-O-acetyl-D-glucopyranose, -2,3,4,6-tetra-O-acetyl-D-galactopyranose, and -2,3,5-tri-O-acetyl-D-xylopyranose via oxidation with selenium dioxide has been elaborated.
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页码:1398 / 1405
页数:7
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