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- W4247646729 endingPage "6757" @default.
- W4247646729 startingPage "6753" @default.
- W4247646729 abstract "Abstract The synthesis of fluorinated compounds and their use as pharmaceutical ingredients or synthetic building blocks have been in the focus of chemical and medicinal research. However, the efficient synthesis of trifluoromethylated nitrogen heterocycles is sometimes challenging. Herein, we disclose a simple aziridination process that relies on the use of amines and novel alkenyl iodonium reagents for the synthesis of strained, trifluoromethylated heterocycles. With the utilization of a newly designed and bench‐stable but highly reactive hypervalent alkenyl iodonium species, these three‐membered‐ring heterocyclic compounds can be efficiently constructed from simple amines under mild conditions in the absence of transition‐metal catalysts. The special reactivity of the new trifluoropropenyl synthon towards nucleophilic centers could be exploited in more general cyclization and alkenylation reactions in the future." @default.
- W4247646729 created "2022-05-12" @default.
- W4247646729 creator A5012453189 @default.
- W4247646729 creator A5021536267 @default.
- W4247646729 creator A5052405884 @default.
- W4247646729 creator A5086253368 @default.
- W4247646729 date "2018-04-30" @default.
- W4247646729 modified "2023-10-09" @default.
- W4247646729 title "Design of Trifluoroalkenyl Iodonium Salts for a Hypervalency‐Aided Alkenylation–Cyclization Strategy: Metal‐Free Construction of Aziridine Rings" @default.
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