Transition‐Metal‐Free LiO <i> <sup>t</sup> </i> Bu‐Promoted Three‐Component Reaction for Efficient Synthesis of Triazolyl (Thio)ureas

ABSTRACT A transition‐metal‐free LiO t Bu‐promoted three‐component reaction for efficient synthesis of the triazolyl (thio)ureas has been reported. This reaction proceeded via the cyclocondensation of nitriles and azides in the presence of a base, followed by the interception of the triazolamine and triazole nitrogen anion intermediate using (thio)carbamoylimidazoles. This method is characterized by being transition‐metal‐free, a broad substrate scope, and mild reaction conditions.

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Journal
Asian Journal of Organic Chemistry
Published
2026-03-01
DOI
https://doi.org/10.1002/ajoc.70375
Primary Topic
Click Chemistry and Applications
Type
article
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article

Transition‐Metal‐Free LiO t Bu‐Promoted Three‐Component Reaction for Efficient Synthesis of Triazolyl (Thio)ureas

W. J. Wang, Chunpeng Qiu, Younan Wang, Zhihao Zuo et al.
Asian Journal of Organic Chemistry
Click Chemistry and Applications
article

Transition‐Metal‐Free LiO t Bu‐Promoted Three‐Component Reaction for Efficient Synthesis of Triazolyl (Thio)ureas

W. J. Wang, Chunpeng Qiu, Younan Wang, Zhihao Zuo, Jingyu Wang
article en

Abstract

ABSTRACT A transition‐metal‐free LiO t Bu‐promoted three‐component reaction for efficient synthesis of the triazolyl (thio)ureas has been reported. This reaction proceeded via the cyclocondensation of nitriles and azides in the presence of a base, followed by the interception of the triazolamine and triazole nitrogen anion intermediate using (thio)carbamoylimidazoles. This method is characterized by being transition‐metal‐free, a broad substrate scope, and mild reaction conditions.

Asian Journal of Organic ChemistryVol. 15(3)
Qufu Normal University (CN)
Openalex Percentile: Top 5%
Click Chemistry and Applications
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