The direct C–H amination of arenes is an important strategy to streamline the discovery and preparation of functional molecules. Herein, we report an operationally simple arene C–H amination reaction that, in contrast to most literature precedent, affords directly the synthetically versatile primary aniline products without relying on protecting group manipulations. Inexpensive Fe(II)-sulfate serves as a convenient catalyst for the transformation. The reaction tolerates a wide scope of arenes, including structurally complex drugs. Importantly, the arene substrates are used as limiting reagents in the transformation. This operationally simple transformation should considerably accelerate the discovery of medicines and functional molecules
Secondary and tertiary alkylamines are privileged substance classes which are often found in pharmac...
Catalytic use of FeCl3 in the presence of glacial AcOH for the direct amidation of acid with amine i...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
The direct C–H amination of arenes is an important strategy to streamline the discovery and preparat...
A novel and efficient Fe-catalyzed direct C-H amination (NH2) of arenes is reported using a new redo...
AbstractA simple and efficient amination of sp3 C–H bonds adjacent to a nitrogen atom in amides was ...
The thesis is focused on hydroxylamine-mediated direct arene C-H amination and C-C amination from be...
A mild, efficient and regioselective method for para-amination of activated arenes has been develope...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
A mild, efficient and regioselective method for para‐amination of activated arenes has been develope...
ABSTRACT: A simple method for direct C−H imidation is reported using a new perester-based self-immol...
New horizons in the utility of azides: The rhodium-catalyzed intermolecular direct C-H amination of ...
It is challenging to develop simple and low cost catalytic systems while maintaining high reactivity...
The selective conversion of carbon-oxygen bonds into carbon-nitrogen bonds to form amines is one of ...
Primary amines are essential constituents of biologically active molecules and versatile intermediat...
Secondary and tertiary alkylamines are privileged substance classes which are often found in pharmac...
Catalytic use of FeCl3 in the presence of glacial AcOH for the direct amidation of acid with amine i...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
The direct C–H amination of arenes is an important strategy to streamline the discovery and preparat...
A novel and efficient Fe-catalyzed direct C-H amination (NH2) of arenes is reported using a new redo...
AbstractA simple and efficient amination of sp3 C–H bonds adjacent to a nitrogen atom in amides was ...
The thesis is focused on hydroxylamine-mediated direct arene C-H amination and C-C amination from be...
A mild, efficient and regioselective method for para-amination of activated arenes has been develope...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
A mild, efficient and regioselective method for para‐amination of activated arenes has been develope...
ABSTRACT: A simple method for direct C−H imidation is reported using a new perester-based self-immol...
New horizons in the utility of azides: The rhodium-catalyzed intermolecular direct C-H amination of ...
It is challenging to develop simple and low cost catalytic systems while maintaining high reactivity...
The selective conversion of carbon-oxygen bonds into carbon-nitrogen bonds to form amines is one of ...
Primary amines are essential constituents of biologically active molecules and versatile intermediat...
Secondary and tertiary alkylamines are privileged substance classes which are often found in pharmac...
Catalytic use of FeCl3 in the presence of glacial AcOH for the direct amidation of acid with amine i...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...