Baptistella Lúcia Helena Brito, Cerchiaro Giselle
Instituto de Química, UNICAMP, CP 6154, 13084-971 Campinas, SP, Brazil.
Carbohydr Res. 2004 Feb 25;339(3):665-71. doi: 10.1016/j.carres.2003.10.026.
A highly stereocontrolled synthesis of a beta-D-ribo-hept-6-ulopyranosuronamide derivative, a useful intermediate for the synthesis of other higher sugars, has been developed using naturally occurring (-)-quinic acid as a chiral starting material. The transformation of carbocycle to carbohydrate, a key step in this sequence, occurred in a one-pot reaction: an ozonolysis carried out under mild conditions.
已经开发出一种高度立体控制的合成方法,以天然存在的(-)-奎尼酸作为手性起始原料,合成β-D-核糖-6-庚酮吡喃糖醛酰胺衍生物,这是合成其他更高糖类的有用中间体。在该反应序列中的关键步骤,即碳环向碳水化合物的转化,是在一锅反应中进行的:在温和条件下进行臭氧分解。