Iridium-Catalyzed Direct C-H Amination with Alkylamines: Facile Oxidative Insertion of Amino Group into Iridacycle

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Described herein is the development of Cp*Ir-(III)-catalyzed direct arene C-H amination using alkylamines as an amino source. This C-N bond formation showcases a notable example of cross-dehydrogenative coupling to install an amino functionality at the ortho-position of benzamide substrates. Mechanistic studies including the isolation of an amine-bound iridacyclic intermediate along with a set of chemical oxidations demonstrated the Ir-catalyzed inner-sphere C-H amination with primary alkylamines for the first time.
Publisher
AMER CHEMICAL SOC
Issue Date
2015-11
Language
English
Article Type
Article
Keywords

TRANSITION-METAL-COMPLEXES; CARBON-NITROGEN BONDS; ROOM-TEMPERATURE; ARYL HALIDES; INTERMOLECULAR AMIDATION; COUPLING REACTIONS; SODIUM PERSULFATE; ORTHO-ARYLATION; N-CHLOROAMINES; SIMPLE ARENES

Citation

ACS Catalysis, v.5, no.11, pp.6665 - 6669

ISSN
2155-5435
DOI
10.1021/acscatal.5b02165
URI
http://hdl.handle.net/10203/207499
Appears in Collection
CH-Journal Papers(저널논문)
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