Preparation of Bicyclopyrazolium Scaffolds and Their Application toward 1,3-Difunctionalization
Abstract A photocatalyzed method for synthesizing 2,3-dihydro-1H-pyrazolo[1,2-a]pyrazol-4-ium compounds from pyrazole and 3-phenylpropyl halides is reported. The strategy employs a formal hydride abstraction process achieved through a stepwise hydrogen atom transfer and oxidative radical–polar crossover process to generate a benzylic carbocation. Capture of the carbocation with pyrazole generates an intermediate N-benzylpyrazole, which undergoes cyclization with a pendant halide to form a fused bicyclic pyrazolium scaffold. We demonstrate that the pyrazolium structure can serve as an intermediate toward accomplishing 1,3-difunctionalization through further reaction with various nucleophiles.
Authors
- Patricia Zhang Musacchio (ORCID: https://orcid.org/0000-0002-0211-1893)
- Yufei Zhang
- Hammed Bisiriyu
Institutions
- University at Buffalo, State University of New York (US)
Publication Details
- Journal
- ACS Organic & Inorganic Au
- Published
- 2026-09-28
- DOI
- https://doi.org/10.1021/acsorginorgau.6c00069
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00