AbstractA simple and efficient amination of sp3 C–H bonds adjacent to a nitrogen atom in amides was introduced. The reaction was catalyzed by cheap and low toxic iron salt and used arylamines as nitrogen source. It provides a straightforward construction of acyclic aminals under mild conditions
A catalytic system for intermolecular benzylic C(sp3)–H amination is developed utilizing 1,2,3,4-tet...
Secondary and tertiary alkylamines are privileged substance classes which are often found in pharmac...
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 ...
It is challenging to develop simple and low cost catalytic systems while maintaining high reactivity...
A direct Fe-catalyzed α-amination of 1,3-dicarbonyl compounds has been accomplished using arylhydrox...
Catalytic use of FeCl3 in the presence of glacial AcOH for the direct amidation of acid with amine i...
Iron-catalyzed intramolecular C–H amination of aliphatic azides has recently emerged as a powerful t...
Novel iron-catalyzed amination reactions of various aryl bromides have been developed for the synthe...
Fe-catalyzed direct dehydrogenative C(3)-functionalization of tertiary arylamines was developed via ...
The direct C–H amination of arenes is an important strategy to streamline the discovery and preparat...
We report a protocol for the synthesis of <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-aminals via direc...
A new direct conversion of aldehydes to amides has been realized, in the presence of iron(III) chlor...
Primary amines are essential constituents of biologically active molecules and versatile intermediat...
An efficient Fe-catalyzed amidation of 1,3-dicarbonyl compounds to α-amidated products through C(sp3...
A catalytic system for intermolecular benzylic C(sp3)–H amination is developed utilizing 1,2,3,4-tet...
Secondary and tertiary alkylamines are privileged substance classes which are often found in pharmac...
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 ...
It is challenging to develop simple and low cost catalytic systems while maintaining high reactivity...
A direct Fe-catalyzed α-amination of 1,3-dicarbonyl compounds has been accomplished using arylhydrox...
Catalytic use of FeCl3 in the presence of glacial AcOH for the direct amidation of acid with amine i...
Iron-catalyzed intramolecular C–H amination of aliphatic azides has recently emerged as a powerful t...
Novel iron-catalyzed amination reactions of various aryl bromides have been developed for the synthe...
Fe-catalyzed direct dehydrogenative C(3)-functionalization of tertiary arylamines was developed via ...
The direct C–H amination of arenes is an important strategy to streamline the discovery and preparat...
We report a protocol for the synthesis of <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-aminals via direc...
A new direct conversion of aldehydes to amides has been realized, in the presence of iron(III) chlor...
Primary amines are essential constituents of biologically active molecules and versatile intermediat...
An efficient Fe-catalyzed amidation of 1,3-dicarbonyl compounds to α-amidated products through C(sp3...
A catalytic system for intermolecular benzylic C(sp3)–H amination is developed utilizing 1,2,3,4-tet...
Secondary and tertiary alkylamines are privileged substance classes which are often found in pharmac...
The manipulation of traditionally unreactive functional groups is of paramount importance in modern ...
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