Iridium(III)-Catalyzed Tandem Annulation of Pyridine-Substituted Anilines and α-Cl Ketones for Obtaining 2-Arylindoles
- 28 September 2020
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 85 (21), 13517-13528
- https://doi.org/10.1021/acs.joc.0c01619
Abstract
A facile and expeditious protocol for the synthesis of 2-arylindoles compounds from readily available N-(2-pyridyl)anilines and commercially available α-Cl ketones through iridium-catalyzed C-H activation and cyclization is reported here. As a complementary approach to the conventional strategies for indole synthesis, the transformation exhibits powerful reactivity, tolerates a large number of functional groups and proceeds in good to excellent yields under mild conditions, providing a straightforward method to access structurally diverse and valuable indole scaffolds. Further, the reaction could be easily scaled up to gram scale.Keywords
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