MIXED ORGANOFLUORINE-ORGANOSILICON CHEMISTRY .6. SYNTHESIS OF GEM-DIFLUORO-C-GLYCOSIDES AND C-DISACCHARIDES FROM ACYLSILANES AND TRINUOROMETHYLTRIMETHYLSIIANE - AN EXPLORATORY-STUDY
T. Brigaud et al., MIXED ORGANOFLUORINE-ORGANOSILICON CHEMISTRY .6. SYNTHESIS OF GEM-DIFLUORO-C-GLYCOSIDES AND C-DISACCHARIDES FROM ACYLSILANES AND TRINUOROMETHYLTRIMETHYLSIIANE - AN EXPLORATORY-STUDY, Tetrahedron letters, 37(34), 1996, pp. 6115-6116
Difluoroenoxysilanes, prepared from acylsilanes and trifluoromethyltri
methylsilane under fluoride activation, were glycosylated by glucal to
yield C-diflnoroglycosides with a difluoromethylene group in place of
the anomeric oxygen. Application of this methodology to a xylose-deri
ved acylsilane led to a C-difluorodisaccharide. Copyright (C) 1996 Pub
lished by Elsevier Science Ltd