Transition Metal Mimetic π-Activation by Cationic Bismuth(III) Catalysts for Allylic C–H Functionalization of Olefins Using C═O and C═N Electrophiles
The discovery and utilization of main-group element catalysts that behave similarly to transition metal (TM) complexes have become increasingly active areas of investigation in recent years. Here, we report a series of Lewis acidic bismuth(III) complexes that allow for the catalytic allylic C(sp<sup>3</sup>)-H functionalization of olefins via an organometallic complexation-assisted deprotonation mechanism to generate products containing new C-C bonds. This heretofore unexplored mode of main-group reactivity was applied to the regioselective functionalization of 1,4-dienes and allylbenzene substrates. Experimental and computational mechanistic studies support the key steps of the proposed catalytic cycle, including the intermediacy of elusive Bi-olefin complexes and allylbismuth species.
Authors
- Christopher Z. Zhao
- Sebastián Martínez (ORCID: https://orcid.org/0000-0003-2574-9344)
- Crispin Lichtenberg (ORCID: https://orcid.org/0000-0002-0176-0939)
- Jacqueline Ramler
- Johannes Schwarzmann
- Ruihan Wang (ORCID: https://orcid.org/0000-0003-0562-2290)
- Yiming Wang (ORCID: https://orcid.org/0009-0008-0618-6113)
Institutions
- Philipps University of Marburg (DE)
- University of Pittsburgh (US)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2024-08-05
- DOI
- https://doi.org/10.1021/jacs.4c06235
- Citations
- 21
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 5.25
Funders
- University of Pittsburgh
- European Commission
- Deutsche Forschungsgemeinschaft
- National Institutes of Health
- University of California, Santa Barbara
- National Institute of General Medical Sciences
- HORIZON EUROPE European Research Council