前往化源商城

Carbohydrate Research 2010-10-13

Bromodimethylsulfonium bromide (BDMS) mediated dithioacetalization of carbohydrates under solvent-free conditions.

Abu T Khan, Md Musawwer Khan

文献索引:Carbohydr. Res. 345(15) , 2139-45, (2010)

全文:HTML全文

摘要

A variety of diethyl dithioacetals of sugars can be prepared in very good yields by the reaction of various monosaccharides with ethanethiol in the presence of 3 mol% bromodimethylsulfonium bromide (BDMS) at 0-5°C. Similarly, dipropyl dithioacetal derivatives can also be obtained in good yields using propanethiol under identical reaction conditions. These dithioacetal derivatives were characterized by per-O-acetylation using silica gel-supported perchloric acid. The significant features of the present protocol are good-to-excellent yields, mild, clean, and solvent-free reaction conditions. This method is extremely suitable for the large-scale preparation of dithioacetal derivatives of various sugars.Copyright © 2010 Elsevier Ltd. All rights reserved.

相关化合物

结构式 名称/CAS号 全部文献
乙硫醇 结构式 乙硫醇
CAS:75-08-1
乙硫醇钠 结构式 乙硫醇钠
CAS:811-51-8
丙硫醇钠 结构式 丙硫醇钠
CAS:6898-84-6
丙硫醇 结构式 丙硫醇
CAS:107-03-9