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.
Authors
- Nobuya Tsuji (ORCID: https://orcid.org/0000-0003-3226-6201)
- Nils Frank
- Markus Leutzsch (ORCID: https://orcid.org/0000-0001-8171-9399)
- Fuxing Shi
- Chendan Zhu
- Benjamin List
Institutions
- Hokkaido University (JP)
- Max-Planck-Institut für Kohlenforschung (DE)
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
Funders
- Deutsche Forschungsgemeinschaft
- Max-Planck-Gesellschaft
- Leibniz-Gemeinschaft