Rh-Catalyzed Formal [3 + 2] Cycloaddition Reactions with Cyclopropenones via Sequential C–H/C–C Bond Activation
The utilization of high-valent metal catalysts to promote cycloaddition reactions involving π bonds through C-C bond activation remains challenging. Despite extensive research, the cycloaddition of aldehydes with cyclopropenones catalyzed by metal complexes has not been documented. Herein, we disclose a novel Rh(III)-catalyzed cycloaddition reaction between cyclopropenones and aldehydes, enabling the efficient synthesis of highly functionalized furanones. A detailed mechanistic investigation was conducted, revealing the likely involvement of a tripodal Rh-carbene intermediate in the catalytic cycle, which facilitates the product release pathway. This reaction exhibits a broad substrate scope, good functional group compatibility, and high atom economy, thereby offering a versatile and general approach to the construction of furanones.
Authors
- Jun‐Tao Cao (ORCID: https://orcid.org/0000-0002-8983-4655)
- Meng Sun (ORCID: https://orcid.org/0000-0003-0257-4174)
- Yi Ren (ORCID: https://orcid.org/0000-0002-3665-700X)
- Wei Sun (ORCID: https://orcid.org/0000-0003-3045-7071)
- Qi Qu (ORCID: https://orcid.org/0000-0002-4870-6606)
Institutions
- Ministry of Education of the People's Republic of China (CN)
- Northwest University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-02-13
- DOI
- https://doi.org/10.1021/acs.orglett.5c00248
- Citations
- 5
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 4.68
Funders
- National Natural Science Foundation of China
- Education Department of Shaanxi Province