137449-26-4Relevant articles and documents
Platinum(II)-catalyzed intermolecular hydroarylation of unactivated alkenes with indoles
Zhang, Zhibin,Wang, Xiang,Widenhoefer, Ross A.
, p. 3717 - 3719 (2006)
Ethylene, α-olefins, and vinyl arenes undergo platinum-catalyzed hydroarylation with substituted indoles in moderate to good yield. The Royal Society of Chemistry 2006.
Rhodium(III)-catalyzed indole synthesis using N-N bond as an internal oxidant
Liu, Baoqing,Song, Chao,Sun, Chao,Zhou, Shuguang,Zhu, Jin
supporting information, p. 16625 - 16631 (2013/12/04)
We report herein a Rh(III)-catalyzed cyclization of N-nitrosoanilines with alkynes for streamlined synthesis of indoles. The synthetic protocol features a distinct internal oxidant, N-N bond, as a reactive handle for catalyst turnover, as well as a hitherto tantalizingly elusive intermolecular redox-neutral manifold, predicated upon C-H activation, for the formation of a five-membered azaheterocycle. The compatibility of seemingly dichotomous acidic and basic conditions ensures reaction versatility for multifarious synthetic contexts. The tolerance of an array of auxiliary functional groups potentially permits predefined, programmable substitution patterns to be incorporated into the indole scaffold. Comprehensive mechanistic studies, under acidic condition, support [RhCp*]2+ as generally the catalyst resting state (switchable to [RhCp*(OOCtBu)]+ under certain circumstance) and C-H activation as the turnover-limiting step. Given the variety of covalent linkages available for the nitroso group, this labile functionality is likely to be harnessed as a generic handle for strikingly diverse coupling reactions.
