Access to Benzo[a]fluoren‐5‐ones via Photoinduced Cyclization of 1,7‐Enynes Under Photocatalyst and Additive‐Free Conditions

ABSTRACT A visible‐light‐initiated sulfonylation/cyclization of 1,7‐enynes with sulfonyl chlorides under photocatalyst and additive‐free conditions was developed. Furthermore, sunlight serves as a viable light source for facilitating this reaction. This protocol is green and features a broad substrate scope. The mechanistic studies indicated that a sulfonyl radical pathway was involved in this process.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2026-03-01
DOI
https://doi.org/10.1002/ajoc.70376
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00
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article

Access to Benzo[a]fluoren‐5‐ones via Photoinduced Cyclization of 1,7‐Enynes Under Photocatalyst and Additive‐Free Conditions

Zhiyong Jiang, Xinyi Guo, Xiaolan Xie, Zhichao Chen
Asian Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
article

Access to Benzo[a]fluoren‐5‐ones via Photoinduced Cyclization of 1,7‐Enynes Under Photocatalyst and Additive‐Free Conditions

Zhiyong Jiang, Xinyi Guo, Xiaolan Xie, Zhichao Chen
article en

Abstract

ABSTRACT A visible‐light‐initiated sulfonylation/cyclization of 1,7‐enynes with sulfonyl chlorides under photocatalyst and additive‐free conditions was developed. Furthermore, sunlight serves as a viable light source for facilitating this reaction. This protocol is green and features a broad substrate scope. The mechanistic studies indicated that a sulfonyl radical pathway was involved in this process.

Asian Journal of Organic ChemistryVol. 15(3)
Quanzhou Normal University (CN), Fujian Agriculture and Forestry University (CN)
Openalex Percentile: Top 8%
Sulfur-Based Synthesis Techniques
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