ChemInform Abstract: Fluorinative α‐Cleavage of Cyclic Ketoximes with Diethylaminosulfur Trifluoride: An Efficient Synthesis of Fluorinated Carbonitriles.
Abstract:Fluorinative α-Cleavage of Cyclic Ketoximes with Diethylaminosulfur Trifluoride: An Efficient Synthesis of Fluorinated Carbonitriles. -The presence of substituents capable of stabilizing a carbocation at the α-position of the oxime is essential for the course of the reaction. Oximes like (X) lacking such substituents afford only complex mixtures. -(KIRIHARA, M.; NIIMI, K.; MOMOSE, T.; Chem. Commun. (Cambridge) (1997) 6, 599-600; Fac. Pharm. Sci., Toyama Med. Pharm. Univ., Sugitani, Toyama 930-01, Japan; EN)
Set email alert for when this publication receives citations?
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.