HIGHLY STEREOSELECTIVE SYNTHESIS OF ARYL C-GLYCOSIDES  

作　　者：蔡孟深 邱东旭 

机构地区：[1]School of Pharmaceutical Sciences, Beijing Medical University, Beijing 100083, PRC

出　　处：《Chinese Science Bulletin》1990年第7期615-616,共2页

基　　金：Project supported by the National Natural Science Foundation of China

摘　　要：Schmidt et al. and Williams et al. reported that the reaction of aryl ethers catalyzed by Lewis acids with O-benzyl glycosyl trichloroacetimidates and pyridyl thioglycosides respectively gave C-aryl-D-glycosides stereoselectively. Looking

关 键 词：PYRIDYL BENZYL catalyzed benzene ACETONE ALLYL LEAVING sugar assigned again 

分 类 号：N[自然科学总论]