The amidation reactions of 8-methylquinolines with azides catalyzed by a cationic rhodium(III) complex proceed efficiently to give quinolin-8-ylmethanamine derivatives in good yields via C(sp<sup>3</sup>)–H bond activation under external oxidant-free conditions. A catalytically competent five-membered rhodacycle has been isolated and characterized, revealing a key intermediate in the catalytic cycle
The Rh(III)-catalyzed C-8 selective direct alkylation and alkynylation of quinoline <i>N</i>-oxides...
We report the direct amidation of arene C–H bonds using sulfonyl azides as the amino source to relea...
We report the direct amidation of arene C–H bonds using sulfonyl azides as the amino source to relea...
The amidation reactions of 8-methylquinolines with azides catalyzed by a cationic rhodium(III) comp...
An efficient copper-catalyzed C-H amidation of 8-methylquinolines with N-fluoroarylsulfonimides via ...
The C–H bond activation of methylquinolines, quinoline, 3-methoxyquinoline, and 3-(trifluoromethyl)q...
Imidate esters and diazo compounds have been established as bifunctional substrates for the construc...
Imidate esters and diazo compounds have been established as bifunctional substrates for the construc...
A Rh(III)-catalyzed direct aldehyde C–H amidation from aldehydes and <i>N</i>-chloroamines, prepared...
A Rh(III)-catalyzed reaction of N-methoxybenzamides and 4-diazoisochroman-3-imines is described. Th...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
Redox-neutral synthesis of isoquinolinium salts via C–H activation of presynthesized or in situ form...
Redox-neutral synthesis of isoquinolinium salts via C–H activation of presynthesized or in situ form...
Redox-neutral synthesis of isoquinolinium salts via C–H activation of presynthesized or in situ form...
The Rh(III)-catalyzed C-8 selective direct alkylation and alkynylation of quinoline <i>N</i>-oxides...
We report the direct amidation of arene C–H bonds using sulfonyl azides as the amino source to relea...
We report the direct amidation of arene C–H bonds using sulfonyl azides as the amino source to relea...
The amidation reactions of 8-methylquinolines with azides catalyzed by a cationic rhodium(III) comp...
An efficient copper-catalyzed C-H amidation of 8-methylquinolines with N-fluoroarylsulfonimides via ...
The C–H bond activation of methylquinolines, quinoline, 3-methoxyquinoline, and 3-(trifluoromethyl)q...
Imidate esters and diazo compounds have been established as bifunctional substrates for the construc...
Imidate esters and diazo compounds have been established as bifunctional substrates for the construc...
A Rh(III)-catalyzed direct aldehyde C–H amidation from aldehydes and <i>N</i>-chloroamines, prepared...
A Rh(III)-catalyzed reaction of N-methoxybenzamides and 4-diazoisochroman-3-imines is described. Th...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
Redox-neutral synthesis of isoquinolinium salts via C–H activation of presynthesized or in situ form...
Redox-neutral synthesis of isoquinolinium salts via C–H activation of presynthesized or in situ form...
Redox-neutral synthesis of isoquinolinium salts via C–H activation of presynthesized or in situ form...
The Rh(III)-catalyzed C-8 selective direct alkylation and alkynylation of quinoline <i>N</i>-oxides...
We report the direct amidation of arene C–H bonds using sulfonyl azides as the amino source to relea...
We report the direct amidation of arene C–H bonds using sulfonyl azides as the amino source to relea...