This paper describes a mild strategy to promote amide arylations. Photoinduced oxidation of a Ni(II) aryl amido intermediate is proposed to facilitate the challenging C–N reductive elimination step at moderate temperatures. Notably, the mildly basic conditions employed facilitate access to a broad scope including protected amino acids, heterocycles, phenols, and sterically hindered substituents. Hence, this work presents an attractive strategy to enable late-stage functionalization of pre-existing amide moieties in commercial drugs and natural products
To date, cleavage of the C-N bond in aromatic amides has been achieved in molecules with a distorted...
We describe the functionalization of α-amino C-H bonds with aryl halides using a combination of nick...
This dissertation describes the development of nickel-catalyzed arylations of amides via amide C–N b...
This paper describes a mild strategy to promote amide arylations. Photoinduced oxidation of a Ni(II)...
A novel Ni-catalyzed reductive amidation of C(sp2)− and C(sp3)−O elect...
Herein, we report a one‐electron strategy for catalytic amide synthesis that enables the direct carb...
Herein, we report a one-electron strategy for catalytic amide synthesis that enables the direct carb...
This work demonstrates the dominance of a Ni(0/II/III) cycle for Ni-photoredox amide arylation, whic...
A novel Ni-catalyzed reductive amidation of C(sp<sup>2</sup>)–O and C(sp<sup>3</sup>)–O electrophi...
Over the past two decades, there have been major developments in transition metal-catalyzed aminatio...
Recent studies have demonstrated that amides can be used in nickel-catalyzed reactions that lead to ...
A long-standing challenge in synthetic chemistry is the development of the transamidation reaction. ...
We report the catalytic alkylation of amide derivatives, which relies on the use of nonprecious meta...
Amides are common functional groups that have been studied for more than a century. They are the key...
Transamidation, or the conversion of one amide to another, is a long-standing challenge in organic s...
To date, cleavage of the C-N bond in aromatic amides has been achieved in molecules with a distorted...
We describe the functionalization of α-amino C-H bonds with aryl halides using a combination of nick...
This dissertation describes the development of nickel-catalyzed arylations of amides via amide C–N b...
This paper describes a mild strategy to promote amide arylations. Photoinduced oxidation of a Ni(II)...
A novel Ni-catalyzed reductive amidation of C(sp2)− and C(sp3)−O elect...
Herein, we report a one‐electron strategy for catalytic amide synthesis that enables the direct carb...
Herein, we report a one-electron strategy for catalytic amide synthesis that enables the direct carb...
This work demonstrates the dominance of a Ni(0/II/III) cycle for Ni-photoredox amide arylation, whic...
A novel Ni-catalyzed reductive amidation of C(sp<sup>2</sup>)–O and C(sp<sup>3</sup>)–O electrophi...
Over the past two decades, there have been major developments in transition metal-catalyzed aminatio...
Recent studies have demonstrated that amides can be used in nickel-catalyzed reactions that lead to ...
A long-standing challenge in synthetic chemistry is the development of the transamidation reaction. ...
We report the catalytic alkylation of amide derivatives, which relies on the use of nonprecious meta...
Amides are common functional groups that have been studied for more than a century. They are the key...
Transamidation, or the conversion of one amide to another, is a long-standing challenge in organic s...
To date, cleavage of the C-N bond in aromatic amides has been achieved in molecules with a distorted...
We describe the functionalization of α-amino C-H bonds with aryl halides using a combination of nick...
This dissertation describes the development of nickel-catalyzed arylations of amides via amide C–N b...