Chiral Phosphoric Acid-Catalyzed Asymmetric Hydrogenolysis of C–O Bonds

CBD) analogs. Preliminary mechanistic experiments and DFT calculations suggested that asymmetric hydrogenolysis proceeded via an enantioselective 1,4-transfer hydrogenation initiation step, followed by an aromatization-driven remote proton transfer and skeletal rearrangement.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-07-27
DOI
https://doi.org/10.1021/jacs.6c11054
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Chiral Phosphoric Acid-Catalyzed Asymmetric Hydrogenolysis of C–O Bonds

Rong‐Zhen Liao, Qing‐Xian Xie, Gao‐Wei Wang, X J Li et al.
Journal of the American Chemical Society
Asymmetric Hydrogenation and Catalysis
article

Chiral Phosphoric Acid-Catalyzed Asymmetric Hydrogenolysis of C–O Bonds

Rong‐Zhen Liao, Qing‐Xian Xie, Gao‐Wei Wang, X J Li, Jinli Chen, Chang‐Bin Yu, Yong‐Gui Zhou
article en

Abstract

CBD) analogs. Preliminary mechanistic experiments and DFT calculations suggested that asymmetric hydrogenolysis proceeded via an enantioselective 1,4-transfer hydrogenation initiation step, followed by an aromatization-driven remote proton transfer and skeletal rearrangement.

Journal of the American Chemical Society
Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), University of Chinese Academy of Sciences (CN), Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China, Dalian Institute of Chemical Physics, National Key Research and Development Program of China
Openalex Percentile: Top 20%
Asymmetric Hydrogenation and Catalysis
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