Mild Water-Extruding C(sp3)–O Bond Functionalization with a Modifiable Pyridinium Salt via Dearomatization/Rearomatization Catalysis
Abstract Despite the abundant C(sp3)–O bond-rich feedstocks in nature, catalytic transformations of these resources remain challenging due to the difficulty of C–O bond cleavage. Available strategies rely heavily on stoichiometric sacrificial oxygen trapping or reducing agents, strong Lewis acids, or harsh conditions. Herein, we report a pyridinium salt-catalyzed functionalization of primary, secondary, and tertiary benzylic, allylic, and propargylic alcohols, saccharides, and cyclopropenyl α-carbinols via an unprecedented dearomatization/rearomatization catalytic paradigm. This protocol features mild conditions and an exceptionally broad substrate scope. Molecular dynamics (MD) simulations and DFT calculations support the unprecedented catalytic mode, paving the way for further developments of this concept.
Authors
- Zhou Zhou-xing
- Qing‐Chuan Zheng (ORCID: https://orcid.org/0000-0003-2978-768X)
- Jinbo Zhao (ORCID: https://orcid.org/0000-0002-5261-7366)
- Xiaohong Shang (ORCID: https://orcid.org/0000-0002-7679-8149)
- Xuemeng Li
- Junliang Zhang (ORCID: https://orcid.org/0000-0002-4636-2846)
- Xue-Ning Wang
- Yuteng Wang
Institutions
- Jilin University (CN)
- Fudan University (CN)
- Changchun University of Technology (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-10-28
- DOI
- https://doi.org/10.1021/acs.orglett.6c03889
- Primary Topic
- Oxidative Organic Chemistry Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Natural Science Foundation of Jilin Province
- National Natural Science Foundation of China
- Jilin University