A novel Ni-catalyzed reductive amidation of C(sp<sup>2</sup>)–O and C(sp<sup>3</sup>)–O electrophiles with isocyanates is described. This umpolung reaction allows for an unconventional preparation of benzamides using simple starting materials and easy-to-handle Ni catalysts
This dissertation describes our efforts toward the total synthesis of N-methyl welwitindolinone B is...
This dissertation describes efforts in the field of nickel-catalyzed amide C–N bond activations and ...
A long-standing challenge in synthetic chemistry is the development of the transamidation reaction. ...
A novel Ni-catalyzed reductive amidation of C(sp2)− and C(sp3)−O elect...
A Ni-catalyzed reductive cross-coupling reaction between two electrophiles, amides and aryl iodides,...
A user-friendly, nickel-catalyzed reductive amidation of unactivated primary, secondary, and tert...
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)...
The reaction of activated phenolic compounds, 2,4,6-triaryloxy-1,3,5-triazine (aryl-triazine ethers)...
Bimolecular nucleophilic substitution SN2 is the earliest and most important means of amination of a...
Transition metal-catalyzed cross-couplings provide a powerful means to assemble carbon–carbon (C–C) ...
Ni-catalyzed electrochemical aryl amination (e-amination) is an attractive, emerging approach to for...
This report describes a three-component, Ni-catalyzed reductive coupling that enables the convergent...
Amide bond formation and transition metal-catalyzed cross-coupling are two of the most frequently us...
Arylation via the cleavage of the ortho C–H bonds by a nickel-catalyzed reaction of aromatic amides ...
This dissertation describes our efforts toward the total synthesis of N-methyl welwitindolinone B is...
This dissertation describes efforts in the field of nickel-catalyzed amide C–N bond activations and ...
A long-standing challenge in synthetic chemistry is the development of the transamidation reaction. ...
A novel Ni-catalyzed reductive amidation of C(sp2)− and C(sp3)−O elect...
A Ni-catalyzed reductive cross-coupling reaction between two electrophiles, amides and aryl iodides,...
A user-friendly, nickel-catalyzed reductive amidation of unactivated primary, secondary, and tert...
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)...
The reaction of activated phenolic compounds, 2,4,6-triaryloxy-1,3,5-triazine (aryl-triazine ethers)...
Bimolecular nucleophilic substitution SN2 is the earliest and most important means of amination of a...
Transition metal-catalyzed cross-couplings provide a powerful means to assemble carbon–carbon (C–C) ...
Ni-catalyzed electrochemical aryl amination (e-amination) is an attractive, emerging approach to for...
This report describes a three-component, Ni-catalyzed reductive coupling that enables the convergent...
Amide bond formation and transition metal-catalyzed cross-coupling are two of the most frequently us...
Arylation via the cleavage of the ortho C–H bonds by a nickel-catalyzed reaction of aromatic amides ...
This dissertation describes our efforts toward the total synthesis of N-methyl welwitindolinone B is...
This dissertation describes efforts in the field of nickel-catalyzed amide C–N bond activations and ...
A long-standing challenge in synthetic chemistry is the development of the transamidation reaction. ...
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