Electronic Activation Enables the Borylation of Alkyl C–H Bonds in Saturated Nitrogen Heterocycles
Catalytic functionalization of C-H bonds is a valuable strategy for the synthesis and diversification of organic compounds. The catalytic borylation of heteroaromatic C-H bonds is well established, but the analogous borylation of alkyl C-H bonds in saturated heterocycles remains underdeveloped. Reactions with improved catalysts recently reported for the borylation of alkyl C-H bonds occurred with a narrow range of such nitrogen heterocycles. Here, we describe a broadly applicable approach to activate C-H bonds in saturated nitrogen heterocycles for iridium-catalyzed borylation by installing a group on nitrogen that increases the reactivity of specific C-H bonds. Mechanistic studies reveal that the electron withdrawing groups accelerate the rate of borylation by enhancing the energetics of multiple steps within the catalytic cycle.
Authors
- Kyan A. D’Angelo (ORCID: https://orcid.org/0000-0002-9688-5143)
- Isaac Furay Yu (ORCID: https://orcid.org/0000-0001-9659-2204)
- John F. Hartwig (ORCID: https://orcid.org/0000-0002-4157-468X)
- R.L. Zheng (ORCID: https://orcid.org/0009-0004-1531-7227)
- Richard T. Wetterer (ORCID: https://orcid.org/0009-0003-4728-0580)
- Melody J. Tang
- Chris La (ORCID: https://orcid.org/0000-0002-9982-133X)
Institutions
- University of California System (US)
- University of California, Berkeley (US)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2025-11-11
- DOI
- https://doi.org/10.1021/jacs.5c15431
- Citations
- 1
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.94