1461634-28-5Relevant articles and documents
Boron-trihalide-promoted regioselective ring-opening reactions of gem-difluorocyclopropyl ketones
Yang, Tang-Po,Li, Qiang,Lin, Jin-Hong,Xiao, Ji-Chang
, p. 1077 - 1079 (2014/01/17)
Boron trihalide-promoted ring-opening reactions of gem-difluorocyclopropyl ketones to give the corresponding β-trifluoromethyl ketones and β-halodifluoromethyl ketones were described. It was found that boron trihalides act as both Lewis acids and nucleophiles and the proximal bond prefers to cleave in this transformation.