Synthesis of 2,3,5-trisubstituted 1 <i>H</i> -pyrroles <i>via</i> formal [3 + 2] cycloaddition of 1-arylpropynes and nitriles and their antiproliferative activities

A base-promoted and precise [3 + 2] cycloaddition strategy has been established to access 2,3,5-trisubstituted 1 H -pyrroles.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-12-10
DOI
https://doi.org/10.1039/d4qo01999g
Citations
2
Primary Topic
Synthesis and Characterization of Pyrroles
Type
article
Field-Weighted Citation Impact
0.50
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article

Synthesis of 2,3,5-trisubstituted 1 H -pyrroles via formal [3 + 2] cycloaddition of 1-arylpropynes and nitriles and their antiproliferative activities

Wen Xiong, Luxiang Yin, Fei Jiang, Xiangchun Shen et al.
2 citations
Organic Chemistry Frontiers
Synthesis and Characterization of Pyrroles
0.50
article

Synthesis of 2,3,5-trisubstituted 1 H -pyrroles via formal [3 + 2] cycloaddition of 1-arylpropynes and nitriles and their antiproliferative activities

Wen Xiong, Luxiang Yin, Fei Jiang, Xiangchun Shen, Ling Li, Sha Wu, Jue Li, Huili Li, Dandan He
article en
2 citations

Abstract

A base-promoted and precise [3 + 2] cycloaddition strategy has been established to access 2,3,5-trisubstituted 1 H -pyrroles.

Organic Chemistry FrontiersVol. 12(4)
Guiyang Medical University (CN), Affiliated Hospital of Guizhou Medical University (CN)
Openalex Percentile: Top 37%
Synthesis and Characterization of Pyrroles
0.50
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