Partial benzylation of methyl .ALPHA.- and .BETA.-D-galactopyranosides.
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概要
- 論文の詳細を見る
Partial benzylation of methyl α-D-galactopyranoside with benzyl chloride and LiOH selectively gave the 2,3,6-tribenzyl ether, while that using KOH or RbOH gave the 2,4,6-isomer as the main product. Methyl β-D-galactopyranoside afforded the 3,4,6-tribenzyl ether predominantly, irrespective of the alkali used.
- 公益社団法人 日本化学会の論文
著者
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Zen Shonosuke
School Of Pharmaceutical Sciences Kitasato University
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Koto Shinkiti
School Of Pharmaceutical Sciences Kitasato University
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Morishima Naohiko
School Of Nursing Kitasato University
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Oshima Megumi
School of Pharmaceutical Sciences, Kitasato University
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Sugimoto Akiko
School of Pharmaceutical Sciences, Kitasato University
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