作者:Ahmad S. Altiti、Stewart Bachan、David R. Mootoo
DOI:10.1021/acs.orglett.6b02284
日期:2016.9.16
A synthesis of glycosphingolipids that centers on the reaction of O- and C-glycosyl crotylstannanes and relatively simple lipid aldehydes is described. The modularity of this strategy and versatility of the crotylation products make this an attractive approach to diverse, highly substituted libraries. The methodology is applied to analogues of the potent imunostimulatory glycolipid KRN7000, including
描述了以O-和C-糖基巴豆基stananes与相对简单的脂质醛的反应为中心的鞘糖脂的合成。这种策略的模块化和crotylation产品的多功能性,使其成为吸引各种高度替代图书馆的有吸引力的方法。该方法学适用于强效免疫刺激性糖脂KRN7000的类似物,包括带有非对映神经酰胺片段和2-酰胺基取代基的O-,亚甲基和氟亚甲基连接的等排体。