<i>N</i>,<i>N</i>‑DisubstitutedAnilines Synthesis through Smiles Rearrangement

Herein, we report a general and mild approach to effectively synthesize N-substituted anilines under metal-free conditions using sulfonyl chlorides and amines. Notably, this approach has shown a wide array of functional group tolerance, operational simplicity, and scalability, making it a useful tool for accessing <i>N</i>,<i>N</i>-disubstituted anilines and functionalized products.

Publication Details

Journal
Figshare
Published
2025-07-23
DOI
https://doi.org/10.1021/acs.joc.5c01125.s001
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00
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article

N,N‑DisubstitutedAnilines Synthesis through Smiles Rearrangement

Figshare
Sulfur-Based Synthesis Techniques
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N,N‑DisubstitutedAnilines Synthesis through Smiles Rearrangement

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Abstract

Herein, we report a general and mild approach to effectively synthesize N-substituted anilines under metal-free conditions using sulfonyl chlorides and amines. Notably, this approach has shown a wide array of functional group tolerance, operational simplicity, and scalability, making it a useful tool for accessing <i>N</i>,<i>N</i>-disubstituted anilines and functionalized products.

Figshare
Openalex Percentile: Top 58%
Sulfur-Based Synthesis Techniques
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<i>N</i>,<i>N</i>‑DisubstitutedAnilines Synthesis through Smiles Rearrangement · Figshare (2025) | TGRS Research Map | TGRS