Fe-catalyzed direct dehydrogenative C(3)-functionalization of tertiary arylamines was developed via activation of the sp<sup>3</sup> C(3)–H bond. The reaction is applicable to both cyclic and acyclic amines. The key process is the catalytic desaturative enamine formation from tertiary amines and position-selective C–C bond formation (addition to nitro olefins) at the β-carbon. Products can be converted to versatile and unique nitrogen-containing molecules
An intramolecular C(sp<sup>3</sup>)–O bond formation has been achieved via PhI(OAc)<sub>2</sub>/Na...
A mild, efficient and regioselective method for para-amination of activated arenes has been develope...
This manuscript details the development of a general and mild protocol for the α-C–H cyanation of te...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
Nitrogen functionality is ubiquitous in biologically active molecules, from naturally occurring alka...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
AbstractA simple and efficient amination of sp3 C–H bonds adjacent to a nitrogen atom in amides was ...
Many enzymes oxidize unactivated aliphatic C-H bonds selectively to form alcohols; however, biologic...
A metal-free method for direct β-C(sp<sup>3</sup>)–H functionalization of aliphatic amine was devel...
A nonenzymatic iron-catalyzed dehydrogenative kinetic resolution of cyclic secondary amines using ai...
C–H bonds are ubiquitous structural units of organic molecules. Although these bonds are generally c...
The functionalization of non-activated C–H bond of cyclic amines is of great importance due to the u...
Transition metal-free intramolecular hydride transfer onto arynes is reported for the first time. Th...
A direct Fe-catalyzed α-amination of 1,3-dicarbonyl compounds has been accomplished using arylhydrox...
The oxidative cross-coupling of carbon-hydrogen (C-H) and nitrogen-hydrogen (N-H) bonds to form carb...
An intramolecular C(sp<sup>3</sup>)–O bond formation has been achieved via PhI(OAc)<sub>2</sub>/Na...
A mild, efficient and regioselective method for para-amination of activated arenes has been develope...
This manuscript details the development of a general and mild protocol for the α-C–H cyanation of te...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
Nitrogen functionality is ubiquitous in biologically active molecules, from naturally occurring alka...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
AbstractA simple and efficient amination of sp3 C–H bonds adjacent to a nitrogen atom in amides was ...
Many enzymes oxidize unactivated aliphatic C-H bonds selectively to form alcohols; however, biologic...
A metal-free method for direct β-C(sp<sup>3</sup>)–H functionalization of aliphatic amine was devel...
A nonenzymatic iron-catalyzed dehydrogenative kinetic resolution of cyclic secondary amines using ai...
C–H bonds are ubiquitous structural units of organic molecules. Although these bonds are generally c...
The functionalization of non-activated C–H bond of cyclic amines is of great importance due to the u...
Transition metal-free intramolecular hydride transfer onto arynes is reported for the first time. Th...
A direct Fe-catalyzed α-amination of 1,3-dicarbonyl compounds has been accomplished using arylhydrox...
The oxidative cross-coupling of carbon-hydrogen (C-H) and nitrogen-hydrogen (N-H) bonds to form carb...
An intramolecular C(sp<sup>3</sup>)–O bond formation has been achieved via PhI(OAc)<sub>2</sub>/Na...
A mild, efficient and regioselective method for para-amination of activated arenes has been develope...
This manuscript details the development of a general and mild protocol for the α-C–H cyanation of te...