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Angewandte Chemie International Edition, 2016-07, Vol.55 (28), p.8113-8116
Auflage
International ed. in English
Ort / Verlag
Germany: Blackwell Publishing Ltd
Erscheinungsjahr
2016
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
A chiral iridium(I) N‐heterocyclic carbene complex was reported for the first time as the catalyst in the highly enantioselective intramolecular allylic amination reaction. The current method provides facile access to biologically important enantioenriched indolopiperazinones and piperazinones in good yields (74–91 %) and excellent enantioselectivities (92–99 % ee). Preliminary mechanistic investigations reveal that the C−H activation occurs at the position ortho to the N‐aryl group of the ligand.
A chiral iridium(I) N‐heterocyclic carbene complex catalyzes highly enantioselective intramolecular allylic amination reactions. This method provides facile access to biologically important enantioenriched indolopiperazinones and piperazinones in good yields. Mechanistic investigations reveal that the C−H activation occurs at the position ortho to the N‐aryl group of the ligand.