Catalytic asymmetric activation of bicyclobutanes

Abstract The precise manipulation of unfunctionalized hydrocarbons remains a fundamental challenge for chemical synthesis and catalysis. Stereodifferentiation in strained alkanes is particularly difficult to accomplish because a catalyst has to distinguish various highly exergonic chemo- and stereoselective strain-release channels. Here we disclose an organocatalytic asymmetric hydroalkoxylation of bicyclobutanes with alcohols to efficiently access tertiary cyclopropylcarbinyl ethers with high enantioselectivity (e.r. up to 98:2). Enantiocontrol is accomplished through chiral recognition between the confined iminoimidodiphosphoric acid catalyst and the substrate, mediated by non-covalent interactions between a Lewis basic binding site of the confined anion and the polarized C–H bond of the cyclopropylcarbinyl ion intermediate. Our work establishes bicyclobutane activation by harnessing strain-release energetics while maintaining precise stereo- and regiocontrol through structural confinement.

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Publication Details

Journal
Nature Synthesis
Published
2026-01-05
DOI
https://doi.org/10.1038/s44160-025-00951-z
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Catalytic asymmetric activation of bicyclobutanes

Nobuya Tsuji, Nils Frank, Markus Leutzsch, Fuxing Shi et al.
Nature Synthesis
Organoboron and organosilicon chemistry
article

Catalytic asymmetric activation of bicyclobutanes

Nobuya Tsuji, Nils Frank, Markus Leutzsch, Fuxing Shi, Chendan Zhu, Benjamin List
article en

Abstract

Abstract The precise manipulation of unfunctionalized hydrocarbons remains a fundamental challenge for chemical synthesis and catalysis. Stereodifferentiation in strained alkanes is particularly difficult to accomplish because a catalyst has to distinguish various highly exergonic chemo- and stereoselective strain-release channels. Here we disclose an organocatalytic asymmetric hydroalkoxylation of bicyclobutanes with alcohols to efficiently access tertiary cyclopropylcarbinyl ethers with high enantioselectivity (e.r. up to 98:2). Enantiocontrol is accomplished through chiral recognition between the confined iminoimidodiphosphoric acid catalyst and the substrate, mediated by non-covalent interactions between a Lewis basic binding site of the confined anion and the polarized C–H bond of the cyclopropylcarbinyl ion intermediate. Our work establishes bicyclobutane activation by harnessing strain-release energetics while maintaining precise stereo- and regiocontrol through structural confinement.

Nature Synthesis
Hokkaido University (JP), Max-Planck-Institut für Kohlenforschung (DE)
Deutsche Forschungsgemeinschaft, Max-Planck-Gesellschaft, Leibniz-Gemeinschaft
Openalex Percentile: Top 98%
Organoboron and organosilicon chemistry
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