Cp*Rh(III) complexes have been applied as efficient catalysts for the C-H activation and trifluoromethylthiolation of indoles functionalized with a heterocycle. With N-trifluoromethylthiosaccharin being an electrophilic SCF3 reagent, this C-S coupling occurred selectively at the 2-position with good functional group tolerance
C-H activation under redox-neutral conditions, especially by Rh(III) catalysis, has offered attracti...
International audienceThe direct dearomative addition of arenes to the C3-position of unprotected in...
International audienceThe direct dearomative addition of arenes to the C3-position of unprotected in...
Cp*Rh(III) complexes have been applied as efficient catalysts for the C–H activation and trifluorom...
A Rh(III)-catalyzed site-selective C-H activation of C(3)-functionalized indoles in a coupling with ...
A Rh(iii)-catalyzed C-H activation of indole at the C4-position leading to novel and switchable func...
A Rh(iii)-catalyzed C-H activation of indole at the C4-position leading to novel and switchable func...
Cp*Co-III-catalyzed directed C-H trifluoromethylthiolation using N-trifluoromethylthiodibenzenesulfo...
Imidate esters and diazo compounds have been established as bifunctional substrates for the construc...
Transition-metal catalyzed C-H functionalizations have impacted and changed synthetic approaches tow...
The direct manipulation of C-H bonds is now a powerful tool in chemical synthesis. In achieving the ...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
A thioether-directed Rh(III)-catalyzed C4 selective C–H alkenylation of indoles via the formation o...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
The rhodium(III)-catalyzed intramolecular annulation of alkyne-tethered acetanilides for the synthes...
C-H activation under redox-neutral conditions, especially by Rh(III) catalysis, has offered attracti...
International audienceThe direct dearomative addition of arenes to the C3-position of unprotected in...
International audienceThe direct dearomative addition of arenes to the C3-position of unprotected in...
Cp*Rh(III) complexes have been applied as efficient catalysts for the C–H activation and trifluorom...
A Rh(III)-catalyzed site-selective C-H activation of C(3)-functionalized indoles in a coupling with ...
A Rh(iii)-catalyzed C-H activation of indole at the C4-position leading to novel and switchable func...
A Rh(iii)-catalyzed C-H activation of indole at the C4-position leading to novel and switchable func...
Cp*Co-III-catalyzed directed C-H trifluoromethylthiolation using N-trifluoromethylthiodibenzenesulfo...
Imidate esters and diazo compounds have been established as bifunctional substrates for the construc...
Transition-metal catalyzed C-H functionalizations have impacted and changed synthetic approaches tow...
The direct manipulation of C-H bonds is now a powerful tool in chemical synthesis. In achieving the ...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
A thioether-directed Rh(III)-catalyzed C4 selective C–H alkenylation of indoles via the formation o...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
The rhodium(III)-catalyzed intramolecular annulation of alkyne-tethered acetanilides for the synthes...
C-H activation under redox-neutral conditions, especially by Rh(III) catalysis, has offered attracti...
International audienceThe direct dearomative addition of arenes to the C3-position of unprotected in...
International audienceThe direct dearomative addition of arenes to the C3-position of unprotected in...
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