A novel, and efficient nickel-catalyzed deoxycyanation of phenolic compounds using relatively nontoxic Zn(CN)2 as the cyanide source was developed. The reaction of C-O bond activated phenolic compounds by 2,4,6-trichloro-1,3,5-triazine with Zn(CN)2 in the presence of a nickel precatalyst afforded the aromatic nitriles in good to excellent yields
A nickel-catalyzed arylcyanation reaction for the synthesis of 3,3-disubstituted oxindoles has been ...
A new method for C–O bond activation of phenolic compounds has been achieved using 2,4,6-trichloro-1...
This manuscript describes the Ni-catalyzed coupling of azoles with aromatic nitriles. The use of BPh...
A novel, and efficient nickel-catalyzed deoxycyanation of phenolic compounds using relatively nontox...
An efficient nickel-catalyzed cyanation of aryl sulfonates, fluorosulfonates, and sulfamates with Zn...
Generation of useful arylnitrile structures from simple aromatic feedstock chemicals represents a fu...
A nickel-catalyzed cyanation of unactivated secondary alkyl chlorides or bromides using less toxic Z...
We report the nickel-catalyzed cyanation and hydrocynation methods to prepare aryl nitriles and viny...
Nitriles are considered very versatile functional groups due to their ability to easily be transform...
Nitriles are considered very versatile functional groups due to their ability to easily be transform...
We describe a nickel‐catalyzed cyanation reaction of aryl (pseudo)halides that employs butyronitrile...
In classic cyanation reactions, toxic metal cyanide sources or complex organic cyanide sources are o...
A nickel-catalyzed cyanation reaction of benzylic and allylic pivalate esters is reported using an a...
An efficient nickel-catalyzed decarbonylative cyanation reaction which allows the direct functional-...
The transition metal-catalysed N-arylation of cyanate salts represents an atom-economical approach t...
A nickel-catalyzed arylcyanation reaction for the synthesis of 3,3-disubstituted oxindoles has been ...
A new method for C–O bond activation of phenolic compounds has been achieved using 2,4,6-trichloro-1...
This manuscript describes the Ni-catalyzed coupling of azoles with aromatic nitriles. The use of BPh...
A novel, and efficient nickel-catalyzed deoxycyanation of phenolic compounds using relatively nontox...
An efficient nickel-catalyzed cyanation of aryl sulfonates, fluorosulfonates, and sulfamates with Zn...
Generation of useful arylnitrile structures from simple aromatic feedstock chemicals represents a fu...
A nickel-catalyzed cyanation of unactivated secondary alkyl chlorides or bromides using less toxic Z...
We report the nickel-catalyzed cyanation and hydrocynation methods to prepare aryl nitriles and viny...
Nitriles are considered very versatile functional groups due to their ability to easily be transform...
Nitriles are considered very versatile functional groups due to their ability to easily be transform...
We describe a nickel‐catalyzed cyanation reaction of aryl (pseudo)halides that employs butyronitrile...
In classic cyanation reactions, toxic metal cyanide sources or complex organic cyanide sources are o...
A nickel-catalyzed cyanation reaction of benzylic and allylic pivalate esters is reported using an a...
An efficient nickel-catalyzed decarbonylative cyanation reaction which allows the direct functional-...
The transition metal-catalysed N-arylation of cyanate salts represents an atom-economical approach t...
A nickel-catalyzed arylcyanation reaction for the synthesis of 3,3-disubstituted oxindoles has been ...
A new method for C–O bond activation of phenolic compounds has been achieved using 2,4,6-trichloro-1...
This manuscript describes the Ni-catalyzed coupling of azoles with aromatic nitriles. The use of BPh...