Visible-Light-Induced Palladium-Mediated Allylic C–H Alkylation Reaction
Direct C-H alkylation is one of the most important C-C bond formation events and is crucial to the efficient assembly of functionalized carbon skeletons in synthetic chemistry. We report herein a photoinduced palladium-catalyzed strategy for the direct alkylation of allylic C-H bonds. The success of this transformation relies on the use of 2-bromo-1,3-dimethylbenzene as a hydrogen atom transfer (HAT) mediator, in combination with a carbon nucleophile, facilitated by a palladium catalyst activated by blue light. Unlike classical Pd(II/0) pathways, this approach leverages the versatile reactivity of Pd(0/I/II) species through visible-light excitation, establishing a robust foundation for the feasibility of this synthetic methodology.
Authors
- Yu Zheng (ORCID: https://orcid.org/0000-0002-1683-5577)
- Kun Huang (ORCID: https://orcid.org/0000-0001-5194-1255)
- Hua Yang (ORCID: https://orcid.org/0000-0002-5518-5255)
- Kai Chen (ORCID: https://orcid.org/0000-0003-1012-0383)
- Xiaoqing Chen (ORCID: https://orcid.org/0000-0002-8768-8965)
- Weidong Lu
Institutions
- Central South University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-09-19
- DOI
- https://doi.org/10.1021/acs.orglett.5c03515
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00