An efficient rhodium-catalyzed method for direct C-H functionalization at the C4 position of unprotected indoles has been developed. The utility of this method is demonstrated by the concise total syntheses of agroclavine and elymoclavine in a divergent manner. These syntheses feature a Pd-catalyzed asymmetric allylic alkylation reaction to assemble the triyclic indole moiety, and a ring-closing metathesis reaction to form the D ring.National Natural Science Foundation of China [21372017, 21402003, 21290183]SCI(E)ARTICLE133664-36671
The substituted indole nucleus [indole is the acronym from indigo (the natural dye) and oleum (used ...
This review highlights the development of palladium-catalyzed C-H and N-H functionalization reaction...
An intramolecular approach towards the regioselective construction of 2,3-diarylated indoles is r...
An efficient rhodium-catalyzed method for direct C–H functionalization at the C4 position of unprote...
C4-decorated indoles feature in a plethora of bioactive and functional compounds of importance to na...
Site-selective direct functionalization of an indole benzenoid core has been a great challenge due t...
The rhodium(III)-catalyzed intramolecular annulation of alkyne-tethered acetanilides for the synthes...
Unprotected indoles are prepared with the title method, which has a wide scope for alkynes. Excellen...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
A highly regioselective functionalization of indole at the C-4 position by employing an aldehyde fun...
Chapter 1. A sequence of research projects beginning with studies in diastereoselective C-H bond fun...
A Rh(III)-catalyzed site-selective C-H activation of C(3)-functionalized indoles in a coupling with ...
An efficient, atom-economic one-pot method was developed for the preparation of 7-substituted indole...
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. A pentamethylcyclopentadienylrhodium(III)-catal...
An efficient strategy for the synthesis of structurally diverse indole-substituted indanones via a r...
The substituted indole nucleus [indole is the acronym from indigo (the natural dye) and oleum (used ...
This review highlights the development of palladium-catalyzed C-H and N-H functionalization reaction...
An intramolecular approach towards the regioselective construction of 2,3-diarylated indoles is r...
An efficient rhodium-catalyzed method for direct C–H functionalization at the C4 position of unprote...
C4-decorated indoles feature in a plethora of bioactive and functional compounds of importance to na...
Site-selective direct functionalization of an indole benzenoid core has been a great challenge due t...
The rhodium(III)-catalyzed intramolecular annulation of alkyne-tethered acetanilides for the synthes...
Unprotected indoles are prepared with the title method, which has a wide scope for alkynes. Excellen...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
A highly regioselective functionalization of indole at the C-4 position by employing an aldehyde fun...
Chapter 1. A sequence of research projects beginning with studies in diastereoselective C-H bond fun...
A Rh(III)-catalyzed site-selective C-H activation of C(3)-functionalized indoles in a coupling with ...
An efficient, atom-economic one-pot method was developed for the preparation of 7-substituted indole...
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. A pentamethylcyclopentadienylrhodium(III)-catal...
An efficient strategy for the synthesis of structurally diverse indole-substituted indanones via a r...
The substituted indole nucleus [indole is the acronym from indigo (the natural dye) and oleum (used ...
This review highlights the development of palladium-catalyzed C-H and N-H functionalization reaction...
An intramolecular approach towards the regioselective construction of 2,3-diarylated indoles is r...