Visible‐Light‐Induced Cyclization of Vinyl Isocyanides with Diaryl Disulfides/1,2‐Dialkyldiselanes for the Synthesis of 1‐Substituted Isoquinolines

Isoquinoline compounds, especially 1‐substituted derivatives, have garnered considerable attention due to their ubiquitous presence in natural products and pharmaceuticals. Herein, a novel visible‐light‐induced tandem cyclization of vinyl isocyanides with diaryl disulfides or 1,2‐dialkyldiselanes has been developed. The reaction tolerates a wide range of substrates and provides an environmentally friendly route to the synthesis of 1‐thio/selenoisoquinolines from the easily available starting materials in a single step.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-10-09
DOI
https://doi.org/10.1002/ejoc.202500715
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.94
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article

Visible‐Light‐Induced Cyclization of Vinyl Isocyanides with Diaryl Disulfides/1,2‐Dialkyldiselanes for the Synthesis of 1‐Substituted Isoquinolines

Xue‐Cen Xu, Qing‐Wen Ai, Yong‐Xin Liang, Yu‐Long Zhao
1 citations
European Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
0.94
article

Visible‐Light‐Induced Cyclization of Vinyl Isocyanides with Diaryl Disulfides/1,2‐Dialkyldiselanes for the Synthesis of 1‐Substituted Isoquinolines

Xue‐Cen Xu, Qing‐Wen Ai, Yong‐Xin Liang, Yu‐Long Zhao
article en
1 citations

Abstract

Isoquinoline compounds, especially 1‐substituted derivatives, have garnered considerable attention due to their ubiquitous presence in natural products and pharmaceuticals. Herein, a novel visible‐light‐induced tandem cyclization of vinyl isocyanides with diaryl disulfides or 1,2‐dialkyldiselanes has been developed. The reaction tolerates a wide range of substrates and provides an environmentally friendly route to the synthesis of 1‐thio/selenoisoquinolines from the easily available starting materials in a single step.

European Journal of Organic ChemistryVol. 28(45)
Northeast Normal University (CN), Qilu Normal University (CN)
Openalex Percentile: Top 21%
Sulfur-Based Synthesis Techniques
0.94
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