An efficient Ir-catalyzed amidation of indoles with sulfonyl azides is disclosed, affording diverse C4-amidated indoles exclusively under mild conditions. In this protocol, a variety of indoles with commonly occurring functional groups such as formyl, acetyl, carboxyl, amide, and ester at the C3 position are well tolerated
Reported herein is the iridium-catalyzed direct amidation of unactivated sp3 C−H bonds. With sulfony...
An efficient and metal-free method for the direct C–N coupling of indoles with azoles to produce 2-(...
C4-decorated indoles feature in a plethora of bioactive and functional compounds of importance to na...
The C4-aminated indole scaffold is frequently encountered in several natural products and biological...
Ir(III)-catalyzed regioselective direct C-7 amidation of indoles in reaction with organic azides has...
Iridium-catalyzed regioselective C-7 amination of indolines has been achieved with organic azides as...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
Iridium-catalyzed direct ortho C-H amidation of arenes has been shown to work well with sulfonyl- an...
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. A pentamethylcyclopentadienylrhodium(III)-catal...
Azidation of indoles using iodine and copper bromide as catalysts under ambient reaction conditions ...
Site-selective direct functionalization of an indole benzenoid core has been a great challenge due t...
Reported herein is the iridium-catalyzed direct amidation of unactivated sp<sup>3</sup> C–H bonds. W...
An iridium-catalyzed direct C-7 selective C–H alkynylation of indolines at room temperature, for the...
An efficient rhodium-catalyzed method for direct C–H functionalization at the C4 position of unprote...
A ruthenium(ii)-catalyzed regioselective direct diamidation of 3-carbonylindoles at the C4- and C5-p...
Reported herein is the iridium-catalyzed direct amidation of unactivated sp3 C−H bonds. With sulfony...
An efficient and metal-free method for the direct C–N coupling of indoles with azoles to produce 2-(...
C4-decorated indoles feature in a plethora of bioactive and functional compounds of importance to na...
The C4-aminated indole scaffold is frequently encountered in several natural products and biological...
Ir(III)-catalyzed regioselective direct C-7 amidation of indoles in reaction with organic azides has...
Iridium-catalyzed regioselective C-7 amination of indolines has been achieved with organic azides as...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
Iridium-catalyzed direct ortho C-H amidation of arenes has been shown to work well with sulfonyl- an...
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. A pentamethylcyclopentadienylrhodium(III)-catal...
Azidation of indoles using iodine and copper bromide as catalysts under ambient reaction conditions ...
Site-selective direct functionalization of an indole benzenoid core has been a great challenge due t...
Reported herein is the iridium-catalyzed direct amidation of unactivated sp<sup>3</sup> C–H bonds. W...
An iridium-catalyzed direct C-7 selective C–H alkynylation of indolines at room temperature, for the...
An efficient rhodium-catalyzed method for direct C–H functionalization at the C4 position of unprote...
A ruthenium(ii)-catalyzed regioselective direct diamidation of 3-carbonylindoles at the C4- and C5-p...
Reported herein is the iridium-catalyzed direct amidation of unactivated sp3 C−H bonds. With sulfony...
An efficient and metal-free method for the direct C–N coupling of indoles with azoles to produce 2-(...
C4-decorated indoles feature in a plethora of bioactive and functional compounds of importance to na...