Synthesis and enantioselective fluorodehydroxylation reactions of (S)-2-(methoxymethyl)pyrrolidin-1-ylsulphur trifluoride, the first homochiral aminofluorosulphurane
Abstract
(S)-2-(Methoxymethyl)pyrrolidin-1-ylsulphur trifluoride (7), the first homochiral aminofluorosulphurane and one of the most stable aminofluorosulphuranes yet reported, has been prepared, and has been shown to be an effective enantioselective fluorodehydroxylating agent.