Intermolecular Ritter-type C–H amination of unactivated sp<sup>3</sup> carbons has been developed. This new reaction proceeds under mild conditions using readily available reagents and an inexpensive source of nitrogen (acetonitrile). A broad scope of substrates can be aminated with this method since many functional groups are tolerated. This reaction also allows for the direct, innate C–H amination of a variety of hydrocarbons such as cyclohexane without the need of prefunctionalization or installation of a directing group
AbstractA simple and efficient amination of sp3 C–H bonds adjacent to a nitrogen atom in amides was ...
A Rh(III)-catalyzed direct aromatic C–H amination is achieved using <i>N</i>-chloroamines as a reage...
C-N Bond formation is of great significance due to the ubiquity of nitrogen-containing compounds. He...
Intermolecular Ritter-type C–H amination of unactivated sp<sup>3</sup> carbons has been developed. T...
A direct Fe-catalyzed α-amination of 1,3-dicarbonyl compounds has been accomplished using arylhydrox...
Elaborating amines via C–H functionalization has been an important area of research over the past de...
International audienceA catalytic intermolecular amination of non-activated tertiary C(sp 3)−H bonds...
Carbon-nitrogen bond formation from inert C-H bonds is an ideal organic transformation and a highly ...
We report a protocol for the synthesis of <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-aminals via direc...
Cross-dehydrogenative couplings (CDCs) have become one of the most straightforward protocols in the ...
Nitrogen functionality is ubiquitous in biologically active molecules, from naturally occurring alka...
Visible light excitation of Iodine (III) - BF3 complex enables the formation of carbocations from C...
Nitrogen functionality is prevalent in synthetic and natural small molecules with significant biolog...
An efficient and convenient method enabling direct amination of unactivated methylene C(sp<sup>3</s...
A metal-free photocatalytic Ritter-type C-H amination of unactivated sp3 carbons using molecular oxy...
AbstractA simple and efficient amination of sp3 C–H bonds adjacent to a nitrogen atom in amides was ...
A Rh(III)-catalyzed direct aromatic C–H amination is achieved using <i>N</i>-chloroamines as a reage...
C-N Bond formation is of great significance due to the ubiquity of nitrogen-containing compounds. He...
Intermolecular Ritter-type C–H amination of unactivated sp<sup>3</sup> carbons has been developed. T...
A direct Fe-catalyzed α-amination of 1,3-dicarbonyl compounds has been accomplished using arylhydrox...
Elaborating amines via C–H functionalization has been an important area of research over the past de...
International audienceA catalytic intermolecular amination of non-activated tertiary C(sp 3)−H bonds...
Carbon-nitrogen bond formation from inert C-H bonds is an ideal organic transformation and a highly ...
We report a protocol for the synthesis of <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-aminals via direc...
Cross-dehydrogenative couplings (CDCs) have become one of the most straightforward protocols in the ...
Nitrogen functionality is ubiquitous in biologically active molecules, from naturally occurring alka...
Visible light excitation of Iodine (III) - BF3 complex enables the formation of carbocations from C...
Nitrogen functionality is prevalent in synthetic and natural small molecules with significant biolog...
An efficient and convenient method enabling direct amination of unactivated methylene C(sp<sup>3</s...
A metal-free photocatalytic Ritter-type C-H amination of unactivated sp3 carbons using molecular oxy...
AbstractA simple and efficient amination of sp3 C–H bonds adjacent to a nitrogen atom in amides was ...
A Rh(III)-catalyzed direct aromatic C–H amination is achieved using <i>N</i>-chloroamines as a reage...
C-N Bond formation is of great significance due to the ubiquity of nitrogen-containing compounds. He...