Bulletin of the Chemical Society of Japan p. 2849 - 2850 (1983)
Update date:2022-08-03
Topics:
Morishima, Naohiko
Koto, Shinkiti
Oshima, Megumi
Sugimoto, Akiko
Zen, Shonosuke
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.
View Morewebsite:http://www.uvchemkeys.com
Contact:0086-021-58785816
Address:RM2607 Building No.1 Guosheng, Lane 388, Zhongjiang Road, Putuo District, Shanghai 200062 China
Nantong LiKai Chemical Co.,Ltd
Contact:+86-513-89068669
Address:Jincheng Science Park
Shuanghe Bio-Technology Limited(expird)
Contact:+86-571-61710758,18968016640
Address:Jinqiao north road 916# Fuyang
Contact:+86 512 6287 2180
Address:398 Ruoshui Road, Suzhou Industrial Park, Suzhou, Jiangsu, P. R. China
Shantou Baokang Pharmaceutical Co., Ltd.
Contact:+86-754-88873487
Address:5/F B Block Huangshan Bldg Huangshan Rd Shantou
Doi:10.1016/j.ejmech.2007.03.031
(2008)Doi:10.1016/j.bmc.2007.10.103
(2008)Doi:10.1021/ol8002095
(2008)Doi:10.1021/jo01065a620
(1961)Doi:10.1016/j.tet.2012.12.037
(2013)Doi:10.1002/anie.202007651
()
