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.

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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

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article

Transition Metal Mimetic π-Activation by Cationic Bismuth(III) Catalysts for Allylic C–H Functionalization of Olefins Using C═O and C═N Electrophiles

Christopher Z. Zhao, Sebastián Martínez, Crispin Lichtenberg, Jacqueline Ramler et al.
21 citations
Journal of the American Chemical Society
Catalytic C–H Functionalization Methods
5.25
article

Transition Metal Mimetic π-Activation by Cationic Bismuth(III) Catalysts for Allylic C–H Functionalization of Olefins Using C═O and C═N Electrophiles

Christopher Z. Zhao, Sebastián Martínez, Crispin Lichtenberg, Jacqueline Ramler, Johannes Schwarzmann, Ruihan Wang, Yiming Wang
article en
21 citations

Abstract

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.

Journal of the American Chemical SocietyVol. 146(32)
Philipps University of Marburg (DE), University of Pittsburgh (US)
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
Openalex Percentile: Top 3%
Catalytic C–H Functionalization Methods
5.25
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Transition Metal Mimetic π-Activation by Cationic Bismuth(III) Catalysts for Allylic C–H Functionalization of Olefins Using C═O and C═N Electrophiles — Christopher Z. Zhao, Sebastián Martínez, et al. · Journal of the American Chemical Society (2024) | TGRS Research Map | TGRS