An iron-catalyzed, 8-amido-enabled regiodivergent C–H allylation of quinolines is described. This reaction represents a rare example of chelation-induced geometrically inaccessible C–H functionalization, allowing for the highly regio- and stereoselective preparation of either the C5- or the C4-allylated quinoline scaffolds regiocontrolled by the catalytic systems
An efficient copper-catalyzed C-H amidation of 8-methylquinolines with N-fluoroarylsulfonimides via ...
Herein, we report a one-pot process that marries mechanistically distinct, traditional cross-couplin...
A highly selective C–H amination reaction under iron catalysis has been developed. This novel system...
An iron-catalyzed, 8-amido-enabled regiodivergent C–H allylation of quinolines is described. This re...
Reported herein is the metal-catalyzed regioselective C-H functionalization of quinoline N-oxides at...
Quinoline is a versatile heterocycle that is part of numerous natural products and countless drugs. ...
A facile and efficient method to synthesize 2- or 4-substituted 1,2-dihydroquinolines and quinolines...
AbstractTransition-metal-catalyzed isoquinoline synthesis that profits from the strategy of chelatio...
The development of new CH functionalization protocols based on inexpensive cobalt catalysts is curr...
A novel and convenient method has been developed for the regioselective iodination of quinolines at ...
Readily available iron(III)-based imidazolium salts have proven to be very versatile catalysts for t...
Reported herein is the metal-catalyzed regioselective C–H functionalization of quinoline <i>N</i>-ox...
The development of new C[BOND]H functionalization protocols based on inexpensive cobalt catalysts is...
A cobalt-catalyzed selective remote C-4 alkylation of 8-aminoquinoline amides via C–H activation und...
The low-valent iron complex Bu<sub>4</sub>N[Fe(CO)<sub>3</sub>(NO)] (<i>TBAFe</i>) catalyzes the a...
An efficient copper-catalyzed C-H amidation of 8-methylquinolines with N-fluoroarylsulfonimides via ...
Herein, we report a one-pot process that marries mechanistically distinct, traditional cross-couplin...
A highly selective C–H amination reaction under iron catalysis has been developed. This novel system...
An iron-catalyzed, 8-amido-enabled regiodivergent C–H allylation of quinolines is described. This re...
Reported herein is the metal-catalyzed regioselective C-H functionalization of quinoline N-oxides at...
Quinoline is a versatile heterocycle that is part of numerous natural products and countless drugs. ...
A facile and efficient method to synthesize 2- or 4-substituted 1,2-dihydroquinolines and quinolines...
AbstractTransition-metal-catalyzed isoquinoline synthesis that profits from the strategy of chelatio...
The development of new CH functionalization protocols based on inexpensive cobalt catalysts is curr...
A novel and convenient method has been developed for the regioselective iodination of quinolines at ...
Readily available iron(III)-based imidazolium salts have proven to be very versatile catalysts for t...
Reported herein is the metal-catalyzed regioselective C–H functionalization of quinoline <i>N</i>-ox...
The development of new C[BOND]H functionalization protocols based on inexpensive cobalt catalysts is...
A cobalt-catalyzed selective remote C-4 alkylation of 8-aminoquinoline amides via C–H activation und...
The low-valent iron complex Bu<sub>4</sub>N[Fe(CO)<sub>3</sub>(NO)] (<i>TBAFe</i>) catalyzes the a...
An efficient copper-catalyzed C-H amidation of 8-methylquinolines with N-fluoroarylsulfonimides via ...
Herein, we report a one-pot process that marries mechanistically distinct, traditional cross-couplin...
A highly selective C–H amination reaction under iron catalysis has been developed. This novel system...