Partial Benzylation of Methyl α- and β-D-Galactopyranosides

DOI: 10.1246/bcsj.56.2849

Source and publish data:

Bulletin of the Chemical Society of Japan p. 2849 - 2850 (1983)

Update date:2022-08-03

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Authors:

Morishima, Naohiko

Koto, Shinkiti

Oshima, Megumi

Sugimoto, Akiko

Zen, Shonosuke

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Article abstract of DOI:10.1246/bcsj.56.2849

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.

Full text of DOI:10.1246/bcsj.56.2849

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