School of Pharmacy, Kitasato University 5-9-1, Shirokane, Minato-ku, Tokyo, Japan.
Carbohydr Res. 2010 Apr 19;345(6):740-9. doi: 10.1016/j.carres.2010.01.011. Epub 2010 Feb 4.
Efficient catalytic and stereoselective glycosylation was achieved by activating a glycosyl N-trichloroacetylcarbamate with a catalytic amount of Lewis acid in the presence of a glycosyl acceptor and 5A molecular sieves. Catalytic one-pot dehydrative glycosylation of a 1-hydroxy carbohydrate was achieved stereoselectively by reaction with trichloroacetyl isocyanate, followed by activation with a catalytic amount of activators.
通过在路易斯酸的催化量存在下,用糖基 N-三氯乙酰基氨基甲酸酯激活糖基受体和 5A 分子筛,实现了高效催化和立体选择性糖基化。通过与三氯乙酰异氰酸酯反应,然后用催化量的活化剂进行活化,立体选择性地实现了 1-羟基糖的催化一锅脱水糖基化。