Catalytic Enantioselective Perezone-Type [5 + 2] Cycloaddition

Here we report the first catalytic enantioselective Perezone-type [5 + 2] cycloaddition, enabling convenient access to a variety of bicyclo[3.2.1]octanes and other complex carbocycles from readily available quinone ketals and alkenes. Enabled by a new chiral squaramide catalyst, intermolecular C-C bond formation was achieved with excellent enantio- and diastereoselectivities. The highly enantioenriched and densely functionalized products can be transformed into diverse intriguing complex carbocycles that may not be straightforward to access by conventional methods. Mechanistic studies and DFT studies provided important insights into the mechanism, in which substrate solvation is a rate-limiting step, while C-C bond formation is fast and stepwise. Activation of the Lewis acid TESOTf by the chiral hydrogen bond donor catalyst is crucial not only for substrate activation and solvation but also for enantiocontrol via the catalyst-bound chiral counter anion.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-10-17
DOI
https://doi.org/10.1021/jacs.5c14484
Citations
1
Primary Topic
Bioactive Compounds and Antitumor Agents
Type
article
Field-Weighted Citation Impact
1.31
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article

Catalytic Enantioselective Perezone-Type [5 + 2] Cycloaddition

Liang‐Liang Yang, Chaoshen Zhang, Jianwei Sun
1 citations
Journal of the American Chemical Society
Bioactive Compounds and Antitumor Agents
1.31
article

Catalytic Enantioselective Perezone-Type [5 + 2] Cycloaddition

Liang‐Liang Yang, Chaoshen Zhang, Jianwei Sun
article en
1 citations

Abstract

Here we report the first catalytic enantioselective Perezone-type [5 + 2] cycloaddition, enabling convenient access to a variety of bicyclo[3.2.1]octanes and other complex carbocycles from readily available quinone ketals and alkenes. Enabled by a new chiral squaramide catalyst, intermolecular C-C bond formation was achieved with excellent enantio- and diastereoselectivities. The highly enantioenriched and densely functionalized products can be transformed into diverse intriguing complex carbocycles that may not be straightforward to access by conventional methods. Mechanistic studies and DFT studies provided important insights into the mechanism, in which substrate solvation is a rate-limiting step, while C-C bond formation is fast and stepwise. Activation of the Lewis acid TESOTf by the chiral hydrogen bond donor catalyst is crucial not only for substrate activation and solvation but also for enantiocontrol via the catalyst-bound chiral counter anion.

Journal of the American Chemical SocietyVol. 147(43)
Hong Kong University of Science and Technology (HK)
Openalex Percentile: Top 18%
Bioactive Compounds and Antitumor Agents
1.31
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Catalytic Enantioselective Perezone-Type [5 + 2] Cycloaddition — Liang‐Liang Yang, Chaoshen Zhang, et al. · Journal of the American Chemical Society (2025) | TGRS Research Map | TGRS