Nickel catalyzed decyanation of aryl and aliphatic cyanides with hydrosilane as the hydride source has been developed. This method is easy to handle, scalable and can be carried out without a glove box. The method has been applied in the cyanide directed functionalization reaction and alpha-substitution of benzyl cyanide
The first efficient and general nickel-catalyzed hydrocyanation of terminal alkynes with Zn(CN)<sub...
Hydrocyanation reactions enable access to synthetically valuable nitriles from readily available alk...
In classic cyanation reactions, toxic metal cyanide sources or complex organic cyanide sources are o...
Nickel catalyzed decyanation of aryl and aliphatic cyanides with hydrosilane as the hydride source h...
Selective hydrogenolysis of C–CN bonds can allow chemists to take advantage of ortho-directing abili...
We report the nickel-catalyzed cyanation and hydrocynation methods to prepare aryl nitriles and viny...
An efficient nickel-catalyzed decarbonylative cyanation reaction which allows the direct functional-...
We describe a nickel‐catalyzed cyanation reaction of aryl (pseudo)halides that employs butyronitrile...
A nickel-catalyzed cyanation of unactivated secondary alkyl chlorides or bromides using less toxic Z...
The in situ generation of a cyano unit from readily available organic precursors is of high interest...
Nitriles are considered very versatile functional groups due to their ability to easily be transform...
Generation of useful arylnitrile structures from simple aromatic feedstock chemicals represents a fu...
Photoinduced nickel-catalyzed demethylative cyanation and decarboxylative cyanomethylation of aryl h...
International audienceHydrosilylation of aldehydes and ketones catalysed by nickel acetate and tricy...
An efficient nickel-catalyzed cyanation of aryl sulfonates, fluorosulfonates, and sulfamates with Zn...
The first efficient and general nickel-catalyzed hydrocyanation of terminal alkynes with Zn(CN)<sub...
Hydrocyanation reactions enable access to synthetically valuable nitriles from readily available alk...
In classic cyanation reactions, toxic metal cyanide sources or complex organic cyanide sources are o...
Nickel catalyzed decyanation of aryl and aliphatic cyanides with hydrosilane as the hydride source h...
Selective hydrogenolysis of C–CN bonds can allow chemists to take advantage of ortho-directing abili...
We report the nickel-catalyzed cyanation and hydrocynation methods to prepare aryl nitriles and viny...
An efficient nickel-catalyzed decarbonylative cyanation reaction which allows the direct functional-...
We describe a nickel‐catalyzed cyanation reaction of aryl (pseudo)halides that employs butyronitrile...
A nickel-catalyzed cyanation of unactivated secondary alkyl chlorides or bromides using less toxic Z...
The in situ generation of a cyano unit from readily available organic precursors is of high interest...
Nitriles are considered very versatile functional groups due to their ability to easily be transform...
Generation of useful arylnitrile structures from simple aromatic feedstock chemicals represents a fu...
Photoinduced nickel-catalyzed demethylative cyanation and decarboxylative cyanomethylation of aryl h...
International audienceHydrosilylation of aldehydes and ketones catalysed by nickel acetate and tricy...
An efficient nickel-catalyzed cyanation of aryl sulfonates, fluorosulfonates, and sulfamates with Zn...
The first efficient and general nickel-catalyzed hydrocyanation of terminal alkynes with Zn(CN)<sub...
Hydrocyanation reactions enable access to synthetically valuable nitriles from readily available alk...
In classic cyanation reactions, toxic metal cyanide sources or complex organic cyanide sources are o...
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