Stereoselective Divergent Synthesis of Chiral Pyrazolone Derivatives via Multicomponent Cascade Reactions by Isothiourea Catalysis

Isothiourea-catalyzed multicomponent cascade reactions are challenging due to the existence of competitive side reactions between multiple reaction partners and intermediates. Herein, we report a practical and efficient protocol for the stereoselective divergent synthesis of pyrazolone-derived β-amino acid esters and β-lactams by isothiourea catalysis. Two distinct reaction pathways are identified, which are controlled by esterification or lactamization of the zwitterionic intermediate. The strategy is attractive because of the convenient one-step procedure, mild conditions, high stereoselectivity, and good functional-group tolerance.

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Publication Details

Journal
Organic Letters
Published
2024-12-26
DOI
https://doi.org/10.1021/acs.orglett.4c04395
Citations
6
Primary Topic
Synthesis of β-Lactam Compounds
Type
article
Field-Weighted Citation Impact
1.50

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article

Stereoselective Divergent Synthesis of Chiral Pyrazolone Derivatives via Multicomponent Cascade Reactions by Isothiourea Catalysis

Shoulei Wang, Liejin Zhou, Xin Liu, Jun Huang et al.
6 citations
Organic Letters
Synthesis of β-Lactam Compounds
1.50
article

Stereoselective Divergent Synthesis of Chiral Pyrazolone Derivatives via Multicomponent Cascade Reactions by Isothiourea Catalysis

Shoulei Wang, Liejin Zhou, Xin Liu, Jun Huang, Siyi Chen, Peiyao Liang
article en
6 citations

Abstract

Isothiourea-catalyzed multicomponent cascade reactions are challenging due to the existence of competitive side reactions between multiple reaction partners and intermediates. Herein, we report a practical and efficient protocol for the stereoselective divergent synthesis of pyrazolone-derived β-amino acid esters and β-lactams by isothiourea catalysis. Two distinct reaction pathways are identified, which are controlled by esterification or lactamization of the zwitterionic intermediate. The strategy is attractive because of the convenient one-step procedure, mild conditions, high stereoselectivity, and good functional-group tolerance.

Organic LettersVol. 27(1)
Fujian Normal University (CN), Zhejiang Normal University (CN), Ministry of Industry and Information Technology (CN)
Fujian Provincial Department of Science and Technology
Openalex Percentile: Top 18%
Synthesis of β-Lactam Compounds
1.50
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