Pd(II)-Catalyzed Site-Selective [2 + 2 + 1] Spiroannulation of 2-Pyridone with Alkyne

Spiropiperidine, an important pharmacophore, is widely found in many drugs and bioactive molecules. Despite the progress these methods have made in the diversity-oriented synthesis of spiropiperidine, site-selective spiroannulation remains a significant challenge. Herein, we report a novel and previously unexplored Pd(II)-catalyzed spiroannulation that uses readily available 2-pyridone as a precursor for piperidine to react with alkyne, undergoing site-selective [2 + 2 + 1] spiroannulation through direct vinylic C-H activation and two metallization steps, efficiently producing 3-spiropiperidine derivatives. This protocol offers a broad substrate scope, strong atom economy, and notable site selectivity and will quickly provide a platform for the diversity-oriented synthesis of 3-spiropiperidine derivatives through the site-selective spiroannulation of conjugated diene.

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Publication Details

Journal
Organic Letters
Published
2026-04-20
DOI
https://doi.org/10.1021/acs.orglett.6c01046
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Pd(II)-Catalyzed Site-Selective [2 + 2 + 1] Spiroannulation of 2-Pyridone with Alkyne

Chenggui Wu, Mingxiang Lu, J Chen, Yunhao Fu et al.
Organic Letters
Catalytic C–H Functionalization Methods
article

Pd(II)-Catalyzed Site-Selective [2 + 2 + 1] Spiroannulation of 2-Pyridone with Alkyne

Chenggui Wu, Mingxiang Lu, J Chen, Yunhao Fu, Long Huang, Yixing Shan, Hui Miao, Longlong Fang, Fan Teng
article en

Abstract

Spiropiperidine, an important pharmacophore, is widely found in many drugs and bioactive molecules. Despite the progress these methods have made in the diversity-oriented synthesis of spiropiperidine, site-selective spiroannulation remains a significant challenge. Herein, we report a novel and previously unexplored Pd(II)-catalyzed spiroannulation that uses readily available 2-pyridone as a precursor for piperidine to react with alkyne, undergoing site-selective [2 + 2 + 1] spiroannulation through direct vinylic C-H activation and two metallization steps, efficiently producing 3-spiropiperidine derivatives. This protocol offers a broad substrate scope, strong atom economy, and notable site selectivity and will quickly provide a platform for the diversity-oriented synthesis of 3-spiropiperidine derivatives through the site-selective spiroannulation of conjugated diene.

Organic LettersVol. 28(17)
Fuyang Normal University (CN), Ministry of Education of the People's Republic of China (CN), Second Military Medical University (CN), Anhui University of Traditional Chinese Medicine (CN), Eastern Hepatobiliary Surgery Hospital (CN), Ministry of Industry and Information Technology (CN)
Anhui University of Chinese Medicine, Anhui Provincial Department of Education, Fuyang Normal University
Openalex Percentile: Top 21%
Catalytic C–H Functionalization Methods
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