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.

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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
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article

Preparation of Bicyclopyrazolium Scaffolds and Their Application toward 1,3-Difunctionalization

Patricia Zhang Musacchio, Yufei Zhang, Hammed Bisiriyu
ACS Organic & Inorganic Au
Radical Photochemical Reactions
article

Preparation of Bicyclopyrazolium Scaffolds and Their Application toward 1,3-Difunctionalization

Patricia Zhang Musacchio, Yufei Zhang, Hammed Bisiriyu
article en

Abstract

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.

ACS Organic & Inorganic Au
University at Buffalo, State University of New York (US)
Openalex Percentile: Top 22%
Radical Photochemical Reactions
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