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2015 Fiscal Year Final Research Report

Development of one step synthesis of glycosyl acceptor substituted by overcrowded silyl group and regioselective glycosidation at 3-OH

Research Project

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Project/Area Number 25410170
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Bio-related chemistry
Research InstitutionSaitama University

Principal Investigator

HATANO Ken  埼玉大学, 理工学研究科, 准教授 (40332316)

Project Period (FY) 2013-04-01 – 2016-03-31
Keywordsシリル基 / グリコシル化 / 位置選択的 / 糖鎖合成
Outline of Final Research Achievements

Silylation of hydroxyl groups on monosaccharides and lactose were obtained in good yield by one step reaction. In the case of lactose, the silylation occurred on 6, 2' and 6' positions of hydroxyl groups and the trisilylated lactose was able to isolate by recrystallization. Regioselective glycosydation at 3-OH (however 3'-OH in the case of lactose) of the silylated saccharides with a glucose derivative as a glycosyl donor were observed.

Free Research Field

有機ケイ素化学

URL: 

Published: 2017-05-10  

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