Visible-Light-Driven Photocatalytic Synthesis of Polysubstituted Pyrrolidines via Desulfurative Tandem Cyclization of Thiols with 1,6-Enynes

A metal-free visible-light photoredox-catalyzed tandem cyclization of 1,6-enynes with thiols was successfully developed. This method provides efficient access to a wide range of five-membered heterocyclic compounds in good to excellent yields with high regioselectivity through a desulfurative/cyclization/HAT process. The versatility of this reaction is demonstrated by its compatibility with a variety of <i>N</i>-tethered 1,6-enynes, encompassing diverse electronic and steric properties. Notably, the cascade reaction demonstrates remarkable operational simplicity, high bond-forming efficiency, and potential scalability, as exemplified by its successful implementation in gram-scale synthesis, which is expected to have potential applications in organic synthesis.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-06-18
DOI
https://doi.org/10.1021/acs.joc.5c00810
Citations
3
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
2.81

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article

Visible-Light-Driven Photocatalytic Synthesis of Polysubstituted Pyrrolidines via Desulfurative Tandem Cyclization of Thiols with 1,6-Enynes

Chongchong Ma, Hongda Xia, Rongshun Chen, Jiangna Yue et al.
3 citations
The Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
2.81
article

Visible-Light-Driven Photocatalytic Synthesis of Polysubstituted Pyrrolidines via Desulfurative Tandem Cyclization of Thiols with 1,6-Enynes

Chongchong Ma, Hongda Xia, Rongshun Chen, Jiangna Yue, Fan Xia, Hengming Yang
article en
3 citations

Abstract

A metal-free visible-light photoredox-catalyzed tandem cyclization of 1,6-enynes with thiols was successfully developed. This method provides efficient access to a wide range of five-membered heterocyclic compounds in good to excellent yields with high regioselectivity through a desulfurative/cyclization/HAT process. The versatility of this reaction is demonstrated by its compatibility with a variety of <i>N</i>-tethered 1,6-enynes, encompassing diverse electronic and steric properties. Notably, the cascade reaction demonstrates remarkable operational simplicity, high bond-forming efficiency, and potential scalability, as exemplified by its successful implementation in gram-scale synthesis, which is expected to have potential applications in organic synthesis.

The Journal of Organic ChemistryVol. 90(26)
Nanjing Agricultural University (CN), Institute of Food Science & Technology (GB)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 10%
Sulfur-Based Synthesis Techniques
2.81
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