A Pragmatic Radical Strategy for Dearomative Hydroalkylation of Unactivated Indoles
Dearomative functionalization offers a direct approach for transforming planar aromatics into C(sp<sup>3</sup>)-rich frameworks with potentially improved drug-like properties. Herein, we report a metal-free and operationally simple method with broad functional group tolerance for the dearomative hydroalkylation of indoles using alkyl boronates. This strategy advances the radical-based dearomatization strategy to previously unreactive indole substrates, enabling access to a variety range of three-dimensional indolines. Notably, it highlights the use of transient indolenium ions in radical-mediated C-C bond formation, establishing a new platform for rapidly diversifying indole-derived scaffolds.
Authors
- Yuzuru Kanda (ORCID: https://orcid.org/0000-0003-2200-2667)
- Tian Qin (ORCID: https://orcid.org/0000-0001-7225-3224)
- Chao Hu (ORCID: https://orcid.org/0000-0003-3237-5934)
- Renzhe Li (ORCID: https://orcid.org/0009-0006-9775-3587)
- Rohan R. Merchant (ORCID: https://orcid.org/0000-0002-5472-8780)
Institutions
- Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
- Novartis (China) (CN)
- Novartis (United States) (US)
- The University of Texas Southwestern Medical Center (US)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1021/jacs.5c17556
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00