Photo‐Induced Sulfonylation/Cyclization of Biaryl Vinyl Ethers with Sulfonyl Chlorides Enabled by Catalytic Triarylamine EDA Complexes: Synthesis of 6 <i>H</i> ‐Benzo[ <i>c</i> ]Chromene Scaffolds

An EDA complex using 4‐methoxy‐ N ‐(4‐methoxyphenyl)‐ N ‐phenylaniline as the catalytic donor for the photo‐induced sulfonylation/cyclization of biaryl vinyl ethers using inexpensive and readily available sulfonyl chlorides has been described. Applying this operationally simple and visible‐light‐mediated general platform, 6 H ‐benzo[ c ]chromene and 6 H ‐benzo[ c ]thiochromene scaffolds can be easily constructed. This protocol tolerated a wide range of functional groups and provided the desired products in 33–86% yields.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-08-15
DOI
https://doi.org/10.1002/adsc.70085
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.94
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article

Photo‐Induced Sulfonylation/Cyclization of Biaryl Vinyl Ethers with Sulfonyl Chlorides Enabled by Catalytic Triarylamine EDA Complexes: Synthesis of 6 H ‐Benzo[ c ]Chromene Scaffolds

Jiangtao Jiang, Min Wang, Haibin Xu, Pinhua Li et al.
1 citations
Advanced Synthesis & Catalysis
Sulfur-Based Synthesis Techniques
0.94
article

Photo‐Induced Sulfonylation/Cyclization of Biaryl Vinyl Ethers with Sulfonyl Chlorides Enabled by Catalytic Triarylamine EDA Complexes: Synthesis of 6 H ‐Benzo[ c ]Chromene Scaffolds

Jiangtao Jiang, Min Wang, Haibin Xu, Pinhua Li, Fengwei Chang, Tiantian Xu
article en
1 citations

Abstract

An EDA complex using 4‐methoxy‐ N ‐(4‐methoxyphenyl)‐ N ‐phenylaniline as the catalytic donor for the photo‐induced sulfonylation/cyclization of biaryl vinyl ethers using inexpensive and readily available sulfonyl chlorides has been described. Applying this operationally simple and visible‐light‐mediated general platform, 6 H ‐benzo[ c ]chromene and 6 H ‐benzo[ c ]thiochromene scaffolds can be easily constructed. This protocol tolerated a wide range of functional groups and provided the desired products in 33–86% yields.

Advanced Synthesis & CatalysisVol. 367(20)
Anhui Polytechnic University (CN)
Openalex Percentile: Top 22%
Sulfur-Based Synthesis Techniques
0.94
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