A Rh(iii)-catalyzed C-H activation of indole at the C4-position leading to novel and switchable functionalization has been reported by employing a weakly co-ordinating COCF3 group as a directing group. An additive plays an important role in switching the selectivity between 1,4-addition products and Heck-type products. An acid additive led to the formation of 1,4-addition products whereas a base additive promotes the formation of Heck-type products. Deuteration studies and control experiments were helpful to propose the mechanism
A site selective C–H aminomethylation at indole’s C3 position has been achieved by merging rhodium(...
Imidate esters and diazo compounds have been established as bifunctional substrates for the construc...
The first example of Rh(III)-catalyzed cyclization of arylnitrones to indolines under external oxida...
A Rh(iii)-catalyzed C-H activation of indole at the C4-position leading to novel and switchable func...
A Rh(III)-catalyzed site-selective C-H activation of C(3)-functionalized indoles in a coupling with ...
Maleimides are not known to undergo oxidative-Heck reaction because they lack a syn-periplanar beta-...
Synthesis of 3-(indol-2-yl)succinimide derivatives is presented using a directing group strategy. Se...
Maleimides are not known to undergo oxidative-Heck reaction because they lack a syn-periplanar beta-...
Synthesis of 3-(indol-2-yl)succinimide derivatives is presented using a directing group strategy. Se...
The rhodium(III)-catalyzed intramolecular annulation of alkyne-tethered acetanilides for the synthes...
The synthesis of N-unprotected indoles has been realized via Rh(III)-catalyzed C-H activation/annula...
C-H activation under redox-neutral conditions, especially by Rh(III) catalysis, has offered attracti...
Chapter 1. A sequence of research projects beginning with studies in diastereoselective C-H bond fun...
Synthesis of 3-(indol-2-yl)succinimide derivatives is presented using a directing group strategy. S...
The possibility of developing new methods for the efficient construction of organic molecules via di...
A site selective C–H aminomethylation at indole’s C3 position has been achieved by merging rhodium(...
Imidate esters and diazo compounds have been established as bifunctional substrates for the construc...
The first example of Rh(III)-catalyzed cyclization of arylnitrones to indolines under external oxida...
A Rh(iii)-catalyzed C-H activation of indole at the C4-position leading to novel and switchable func...
A Rh(III)-catalyzed site-selective C-H activation of C(3)-functionalized indoles in a coupling with ...
Maleimides are not known to undergo oxidative-Heck reaction because they lack a syn-periplanar beta-...
Synthesis of 3-(indol-2-yl)succinimide derivatives is presented using a directing group strategy. Se...
Maleimides are not known to undergo oxidative-Heck reaction because they lack a syn-periplanar beta-...
Synthesis of 3-(indol-2-yl)succinimide derivatives is presented using a directing group strategy. Se...
The rhodium(III)-catalyzed intramolecular annulation of alkyne-tethered acetanilides for the synthes...
The synthesis of N-unprotected indoles has been realized via Rh(III)-catalyzed C-H activation/annula...
C-H activation under redox-neutral conditions, especially by Rh(III) catalysis, has offered attracti...
Chapter 1. A sequence of research projects beginning with studies in diastereoselective C-H bond fun...
Synthesis of 3-(indol-2-yl)succinimide derivatives is presented using a directing group strategy. S...
The possibility of developing new methods for the efficient construction of organic molecules via di...
A site selective C–H aminomethylation at indole’s C3 position has been achieved by merging rhodium(...
Imidate esters and diazo compounds have been established as bifunctional substrates for the construc...
The first example of Rh(III)-catalyzed cyclization of arylnitrones to indolines under external oxida...