Modular Synthesis of 3,3-Disubstituted Azetidines via Azetidinylation Reagents

Azetidines represent an attractive and emerging design option in medicinal chemistry owing to their small size and polar nature, as well as their potential to significantly impact the physicochemical properties of drug molecules. However, traditional methods for the synthesis of 3,3-disubstituted azetidines usually require higher step counts or exhibit poor functional group compatibility. Herein, we report a modular synthesis strategy for 3,3-disubstituted azetidines based on azetidinylation reagents. The practicality of this method is further exemplified by the use of readily available starting materials, mild reaction conditions, and a very broad substrate scope.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-03-19
DOI
https://doi.org/10.1021/acs.joc.5c00341
Citations
4
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
3.74

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article

Modular Synthesis of 3,3-Disubstituted Azetidines via Azetidinylation Reagents

Xinru Wang, Yingying Zhang
4 citations
The Journal of Organic Chemistry
Synthesis and Catalytic Reactions
3.74
article

Modular Synthesis of 3,3-Disubstituted Azetidines via Azetidinylation Reagents

Xinru Wang, Yingying Zhang
article en
4 citations

Abstract

Azetidines represent an attractive and emerging design option in medicinal chemistry owing to their small size and polar nature, as well as their potential to significantly impact the physicochemical properties of drug molecules. However, traditional methods for the synthesis of 3,3-disubstituted azetidines usually require higher step counts or exhibit poor functional group compatibility. Herein, we report a modular synthesis strategy for 3,3-disubstituted azetidines based on azetidinylation reagents. The practicality of this method is further exemplified by the use of readily available starting materials, mild reaction conditions, and a very broad substrate scope.

The Journal of Organic ChemistryVol. 90(12)
Huaibei Normal University (CN)
Anhui Provincial Department of Education
Openalex Percentile: Top 8%
Synthesis and Catalytic Reactions
3.74
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