193149-55-2Relevant academic research and scientific papers
Highly Stereoselective Introduction of Fluorine-Containing Methyl Groups at 2 Position of D-Glucose
Hiraoka, Shuichi,Yamazaki, Takashi,Kitazume, Tomoya
, p. 669 - 670 (1997)
Highly stereoselective introduction of fluorine-containing methyl groups at the 2 position of methyl glucoside was attained by use of the difluoromethylene derivative as a key intermediate via hydrogenation of exo- and endo-olefins, whose diastereofacial selectivity was considered to be governed by the anomeric methoxy group.
