A direct Fe-catalyzed α-amination of 1,3-dicarbonyl compounds has been accomplished using arylhydroxylamines as aminating agents. This novel protocol allows convenient access to α-amino carbonyl derivatives without the need for any postreaction manipulations. This is an operationally simple procedure that works at low temperatures in shorter reaction times and produces high yields with excellent N-selectivity
Fe-catalyzed direct dehydrogenative C(3)-functionalization of tertiary arylamines was developed via ...
Here we report the catalytic transfer hydrogenation (CTH) of non-activated imines promoted by a Fe-c...
A direct α-amination of β-dicarbonyl compounds has been achieved by using iodosobenzene (PhIO) as an...
AbstractA simple and efficient amination of sp3 C–H bonds adjacent to a nitrogen atom in amides was ...
It is challenging to develop simple and low cost catalytic systems while maintaining high reactivity...
Intermolecular Ritter-type C–H amination of unactivated sp<sup>3</sup> carbons has been developed. T...
A highly selective C–H amination reaction under iron catalysis has been developed. This novel system...
An efficient Fe-catalyzed amidation of 1,3-dicarbonyl compounds to α-amidated products through C(sp3...
International audienceAn efficient method for the reductive amination of carbonyl derivatives with ω...
A novel and efficient Fe-catalyzed direct C-H amination (NH2) of arenes is reported using a new redo...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
Secondary and tertiary alkylamines are privileged substance classes which are often found in pharmac...
Methods for the synthesis and functionalization of amines are intrinsically important to a variety o...
International audienceThe first iron catalysts able to promote the formal insertion of CO into the C...
Methods for the synthesis and functionalization of amines are intrinsically important to a variety o...
Fe-catalyzed direct dehydrogenative C(3)-functionalization of tertiary arylamines was developed via ...
Here we report the catalytic transfer hydrogenation (CTH) of non-activated imines promoted by a Fe-c...
A direct α-amination of β-dicarbonyl compounds has been achieved by using iodosobenzene (PhIO) as an...
AbstractA simple and efficient amination of sp3 C–H bonds adjacent to a nitrogen atom in amides was ...
It is challenging to develop simple and low cost catalytic systems while maintaining high reactivity...
Intermolecular Ritter-type C–H amination of unactivated sp<sup>3</sup> carbons has been developed. T...
A highly selective C–H amination reaction under iron catalysis has been developed. This novel system...
An efficient Fe-catalyzed amidation of 1,3-dicarbonyl compounds to α-amidated products through C(sp3...
International audienceAn efficient method for the reductive amination of carbonyl derivatives with ω...
A novel and efficient Fe-catalyzed direct C-H amination (NH2) of arenes is reported using a new redo...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
Secondary and tertiary alkylamines are privileged substance classes which are often found in pharmac...
Methods for the synthesis and functionalization of amines are intrinsically important to a variety o...
International audienceThe first iron catalysts able to promote the formal insertion of CO into the C...
Methods for the synthesis and functionalization of amines are intrinsically important to a variety o...
Fe-catalyzed direct dehydrogenative C(3)-functionalization of tertiary arylamines was developed via ...
Here we report the catalytic transfer hydrogenation (CTH) of non-activated imines promoted by a Fe-c...
A direct α-amination of β-dicarbonyl compounds has been achieved by using iodosobenzene (PhIO) as an...