Well‐Defined [CpCo(N,O)I]‐Catalysts for Site‐Selective Intramolecular C−H Amidation

We present an efficient method for forming C−N bonds via intramolecular amidation catalyzed by well‐defined Cp*Co(N,O)I complexes. The reaction has been operate under mild conditions and produced a regioselective amidation product without the use of a bulky counter anion or expensive fluorinated sol...

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Veröffentlicht in:Advanced synthesis & catalysis 2022-08, Vol.364 (15), p.2642-2647
Hauptverfasser: Dahiya, Pardeep, Sarkar, Ankita, Sundararaju, Basker
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Sarkar, Ankita
Sundararaju, Basker
description We present an efficient method for forming C−N bonds via intramolecular amidation catalyzed by well‐defined Cp*Co(N,O)I complexes. The reaction has been operate under mild conditions and produced a regioselective amidation product without the use of a bulky counter anion or expensive fluorinated solvents. The Cp*Co(N,O)‐I catalyst is very effective for intramolecular benzylic, tertiary, and internal C(sp3)−H bond amidation, but ineffective for intramolecular C(sp2)−H bond amidation.
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subjects Amidation
Catalysts
Cobalt
C−N bond formation
Heterocycles
Hydrogen bonds
Redox-active ligand
title Well‐Defined [CpCo(N,O)I]‐Catalysts for Site‐Selective Intramolecular C−H Amidation
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