Asymmetric Formal Synthesis of (−)-Paroxetine

A concise, asymmetric formal synthesis of (-)-paroxetine is reported. The synthetic strategy features an asymmetric hydrogenation for constructing the chiral center and a phosphate-group-involved intramolecular S<sub>N</sub>2 reaction for the construction of the <i>trans</i>-3,4-disubstituted piperidine scaffold. This synthetic route is concise and practical for (-)-paroxetine synthesis.

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Publication Details

Journal
Organic Letters
Published
2025-05-19
DOI
https://doi.org/10.1021/acs.orglett.5c01622
Citations
1
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.94

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article

Asymmetric Formal Synthesis of (−)-Paroxetine

Sunliang Cui, Lei Liu, Xianjing Zhou, Wen-Feng Huang
1 citations
Organic Letters
Asymmetric Synthesis and Catalysis
0.94
article

Asymmetric Formal Synthesis of (−)-Paroxetine

Sunliang Cui, Lei Liu, Xianjing Zhou, Wen-Feng Huang
article en
1 citations

Abstract

A concise, asymmetric formal synthesis of (-)-paroxetine is reported. The synthetic strategy features an asymmetric hydrogenation for constructing the chiral center and a phosphate-group-involved intramolecular S<sub>N</sub>2 reaction for the construction of the <i>trans</i>-3,4-disubstituted piperidine scaffold. This synthetic route is concise and practical for (-)-paroxetine synthesis.

Organic LettersVol. 27(21)
Jinhua Academy of Agricultural Sciences (CN), Zhejiang University (CN)
National Natural Science Foundation of China, National Program for Support of Top-notch Young Professionals, Natural Science Foundation of Zhejiang Province
Zero hunger
Openalex Percentile: Top 26%
Asymmetric Synthesis and Catalysis
0.94
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Asymmetric Formal Synthesis of (−)-Paroxetine — Sunliang Cui, Lei Liu, et al. · Organic Letters (2025) | TGRS Research Map | TGRS