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.

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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

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article

Mild Water-Extruding C(sp3)–O Bond Functionalization with a Modifiable Pyridinium Salt via Dearomatization/Rearomatization Catalysis

Zhou Zhou-xing, Qing‐Chuan Zheng, Jinbo Zhao, Xiaohong Shang et al.
1 links
Organic Letters
Oxidative Organic Chemistry Reactions
article

Mild Water-Extruding C(sp3)–O Bond Functionalization with a Modifiable Pyridinium Salt via Dearomatization/Rearomatization Catalysis

Zhou Zhou-xing, Qing‐Chuan Zheng, Jinbo Zhao, Xiaohong Shang, Xuemeng Li, Junliang Zhang, Xue-Ning Wang, Yuteng Wang
article en

Abstract

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.

Organic Letters
Jilin University (CN), Fudan University (CN), Changchun University of Technology (CN)
Natural Science Foundation of Jilin Province, National Natural Science Foundation of China, Jilin University
Openalex Percentile: Top 26%
Oxidative Organic Chemistry Reactions
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