Versatile acetylation of carbohydrate substrates with bench-top sulfonic acids and application to one-pot syntheses of peracetylated thioglycosides

被引:44
作者
Chao, Chin-Sheng [1 ]
Chen, Min-Chun [1 ]
Lin, Shih-Che [1 ]
Mong, Kwok-Kong T. [1 ]
机构
[1] Natl Chiao Tung Univ, Dept Appl Chem, Hsinchu 300, Taiwan
关键词
p-toluenesulfonic acid; acid-catalyzed acetylation; amino sugars; one-pot protecting group manipulation;
D O I
10.1016/j.carres.2008.01.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inexpensive and readily available sulfonic acids, p-toluenesulfonic acid, and sulfuric acid are versatile and efficient catalysts for the peracetylation of a broad spectrum of carbohydrate substrates in good yield and in a practical time frame. Three appealing features in sulfonic acid-catalyzed acetylation of free sugars were explored including (1) suppression of furanosyl acetate formation for D-galactose and L-fucose; (2) high yielding chemoselective acetylation of sialic acid under appropriate conditions; and (3) peracetylation of amino sugars with different amino protecting functions. Simple one-pot two step acetylation-thioglycosidation methods for the expeditious synthesis of p-tolyl per-O-acetyl thioglycosides were also delineated. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:957 / 964
页数:8
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