A novel procedure for the NiCl<sub>2</sub>(DME)/dppp/Zn system catalyzed intermolecular insertion of aryl iodides to nitriles was developed, which afforded variously substituted arylketone derivatives in moderate to good yields with tolerance of a wide variety of functional groups
Carbon-Carbon cross-coupling is a useful method that is used to connect carbons of different molecul...
A catalytic amount of NidppeCl(2) converts an acyl bromide directly into ketones at 0 degrees C in T...
The complex [Ni(acac)2] (Hacac = pentane-2,4-dione) selectively catalyses addition of the intercarbo...
[[abstract]]Aryl iodides (ArI) couple with aryl aldehydes (Ar'CHO) in the presence of Ni(dppe)Br-2 a...
The catalytic intermolecular arylation of disubstituted geminal dinitriles with in situ generated ar...
Through a nickel-catalysed Heck-type reaction, a direct coupling of alkenes with alpha-cyano alkyl b...
The present work highlights unprecedented Ni-catalyzed reductive coupling of unactivated alkyl iodid...
The catalytic intermolecular arylation of disubstituted geminal dinitriles with in situ generated ar...
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...
This manuscript describes the Ni-catalyzed coupling of azoles with aromatic nitriles. The use of BPh...
A nickel-catalyzed arylcyanation reaction for the synthesis of 3,3-disubstituted oxindoles has been ...
This manuscript describes the Ni-catalyzed coupling of azoles with aromatic nitriles. The use of BPh...
Chapter one provides a survey of the wide variety of unconventional phenol derivatives that are now ...
An efficient nickel-catalyzed intramolecular direct arylation of imines with challenging aryl chlori...
Carbon-Carbon cross-coupling is a useful method that is used to connect carbons of different molecul...
A catalytic amount of NidppeCl(2) converts an acyl bromide directly into ketones at 0 degrees C in T...
The complex [Ni(acac)2] (Hacac = pentane-2,4-dione) selectively catalyses addition of the intercarbo...
[[abstract]]Aryl iodides (ArI) couple with aryl aldehydes (Ar'CHO) in the presence of Ni(dppe)Br-2 a...
The catalytic intermolecular arylation of disubstituted geminal dinitriles with in situ generated ar...
Through a nickel-catalysed Heck-type reaction, a direct coupling of alkenes with alpha-cyano alkyl b...
The present work highlights unprecedented Ni-catalyzed reductive coupling of unactivated alkyl iodid...
The catalytic intermolecular arylation of disubstituted geminal dinitriles with in situ generated ar...
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...
This manuscript describes the Ni-catalyzed coupling of azoles with aromatic nitriles. The use of BPh...
A nickel-catalyzed arylcyanation reaction for the synthesis of 3,3-disubstituted oxindoles has been ...
This manuscript describes the Ni-catalyzed coupling of azoles with aromatic nitriles. The use of BPh...
Chapter one provides a survey of the wide variety of unconventional phenol derivatives that are now ...
An efficient nickel-catalyzed intramolecular direct arylation of imines with challenging aryl chlori...
Carbon-Carbon cross-coupling is a useful method that is used to connect carbons of different molecul...
A catalytic amount of NidppeCl(2) converts an acyl bromide directly into ketones at 0 degrees C in T...
The complex [Ni(acac)2] (Hacac = pentane-2,4-dione) selectively catalyses addition of the intercarbo...