The nickel-catalyzed cross-electrophile coupling of aryl halides and alkyl halides enabled by ball-milling is herein described. Under a mechanochemical manifold, the reductive C–C bond formation was achieved in the absence of bulk solvent and air/moisture sensitive setups, in reaction times of 2 h. The mechanical action provided by ball milling permits the use of a range of zinc sources to turnover the nickel catalytic cycle, enabling the synthesis of 28 cross-electrophile coupled products
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...
The nickel-catalyzed cross-electrophile coupling of aryl halides and alkyl halides enabled by ball-m...
The nickel-catalyzed cross-electrophile coupling of aryl halides and alkyl halides enabled by ball-m...
The nickel-catalyzed cross-electrophile coupling of aryl halides and alkyl halides enabled by ball-m...
The cross-electrophile coupling of either twisted-amides or heteroaryl halides with alkyl halides, e...
The cross-electrophile coupling of either twisted-amides or heteroaryl halides with alkyl halides, e...
The cross-electrophile coupling of either twisted-amides or heteroaryl halides with alkyl halides, e...
The cross-electrophile coupling of either twisted-amides or heteroaryl halides with alkyl halides, e...
This thesis describes the investigations into solvent-minimised catalytic transformations, under m...
This thesis describes the investigations into solvent-minimised catalytic transformations, under m...
Activating raw, zero-valent metals is an essential capability for chemical processes, which include ...
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...
The use of temperature-controlled mechanochemistry to enable the mechanochemical nickel-catalyzed Su...
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...
The nickel-catalyzed cross-electrophile coupling of aryl halides and alkyl halides enabled by ball-m...
The nickel-catalyzed cross-electrophile coupling of aryl halides and alkyl halides enabled by ball-m...
The nickel-catalyzed cross-electrophile coupling of aryl halides and alkyl halides enabled by ball-m...
The cross-electrophile coupling of either twisted-amides or heteroaryl halides with alkyl halides, e...
The cross-electrophile coupling of either twisted-amides or heteroaryl halides with alkyl halides, e...
The cross-electrophile coupling of either twisted-amides or heteroaryl halides with alkyl halides, e...
The cross-electrophile coupling of either twisted-amides or heteroaryl halides with alkyl halides, e...
This thesis describes the investigations into solvent-minimised catalytic transformations, under m...
This thesis describes the investigations into solvent-minimised catalytic transformations, under m...
Activating raw, zero-valent metals is an essential capability for chemical processes, which include ...
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...
The use of temperature-controlled mechanochemistry to enable the mechanochemical nickel-catalyzed Su...
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...
Nickel-catalyzed selective cross-coupling of aromatic electrophiles (bromides, chlorides, fluorides ...