We report the catalytic alkylation of amide derivatives, which relies on the use of nonprecious metal catalysis. Amide derivatives are treated with organozinc reagents, utilizing nickel catalysis, to yield ketone products. The methodology is performed at ambient temperature and is tolerant of variation in both coupling partners. A precursor to a nanomolar glucagon receptor modulator was synthesized using the methodology, underscoring the mild nature of this chemistry and its potential utility in pharmaceutical synthesis. These studies are expected to further promote the use of amides as synthetic building blocks
A user-friendly, nickel-catalyzed reductive amidation of unactivated primary, secondary, and tert...
A long-standing challenge in synthetic chemistry is the development of the transamidation reaction. ...
We report the Ni-catalyzed Suzuki–Miyaura coupling of aliphatic amide derivatives. Prior studies hav...
This dissertation describes efforts in the field of nickel-catalyzed amide C–N bond activations and ...
A protocol for the nickel-catalyzed alkylation of amides was established. The use of alkylboranes as...
Transamidation, or the conversion of one amide to another, is a long-standing challenge in organic s...
Herein, we developed an operational simple, practical, and selective Ni-catalyzed synthesis of secon...
Recent studies have demonstrated that amides can be used in nickel-catalyzed reactions that lead to ...
This dissertation is divided into two main themes concerning transition metal-mediatedmethodologies ...
This dissertation describes the development of nickel-catalyzed arylations of amides via amide C–N b...
Suzuki−Miyaura cross-couplings of amides offer an approach to the synthesis of ketones that avoids t...
A general Negishi acylation of primary amides enabled by a combination of site-selective <i>N</i>,<i...
Amides are common functional groups that have been studied for more than a century. They are the key...
This paper describes a mild strategy to promote amide arylations. Photoinduced oxidation of a Ni(II)...
Nickel-catalyzed amidation of aryl alkynyl acids using tetraalkylthiuram disulfides as the amine sou...
A user-friendly, nickel-catalyzed reductive amidation of unactivated primary, secondary, and tert...
A long-standing challenge in synthetic chemistry is the development of the transamidation reaction. ...
We report the Ni-catalyzed Suzuki–Miyaura coupling of aliphatic amide derivatives. Prior studies hav...
This dissertation describes efforts in the field of nickel-catalyzed amide C–N bond activations and ...
A protocol for the nickel-catalyzed alkylation of amides was established. The use of alkylboranes as...
Transamidation, or the conversion of one amide to another, is a long-standing challenge in organic s...
Herein, we developed an operational simple, practical, and selective Ni-catalyzed synthesis of secon...
Recent studies have demonstrated that amides can be used in nickel-catalyzed reactions that lead to ...
This dissertation is divided into two main themes concerning transition metal-mediatedmethodologies ...
This dissertation describes the development of nickel-catalyzed arylations of amides via amide C–N b...
Suzuki−Miyaura cross-couplings of amides offer an approach to the synthesis of ketones that avoids t...
A general Negishi acylation of primary amides enabled by a combination of site-selective <i>N</i>,<i...
Amides are common functional groups that have been studied for more than a century. They are the key...
This paper describes a mild strategy to promote amide arylations. Photoinduced oxidation of a Ni(II)...
Nickel-catalyzed amidation of aryl alkynyl acids using tetraalkylthiuram disulfides as the amine sou...
A user-friendly, nickel-catalyzed reductive amidation of unactivated primary, secondary, and tert...
A long-standing challenge in synthetic chemistry is the development of the transamidation reaction. ...
We report the Ni-catalyzed Suzuki–Miyaura coupling of aliphatic amide derivatives. Prior studies hav...