Evidence map›Paper›PMID 41265637›Full record

ArticleJournal of advanced research2026

Reactions of N-heterocyclic carbenes with nitrobenzenes: harnessing NHCs as synthetic building blocks.

Zhiguo Zheng, Youlin Deng, Xiaoqun Yang, Zhichao Jin, Shiqing Huang, Jian Wu, Yonggui Robin Chi

Abstract read
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Article in Journal of advanced research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Zhiguo ZhengState Key Laboratory of Green Pesticide, Guizhou University, Guiyang 550025, China.
Youlin DengState Key Laboratory of Green Pesticide, Guizhou University, Guiyang 550025, China.
Xiaoqun YangState Key Laboratory of Green Pesticide, Guizhou University, Guiyang 550025, China.
Zhichao JinState Key Laboratory of Green Pesticide, Guizhou University, Guiyang 550025, China.
Shiqing HuangSchool of Chemistry and Life Resources, Renmin University of China, Beijing 100872, China; School of Chemistry, Chemical Engineering, and Biotechnology, Nanyang Technological University, Singapore 637371 Singapore. Electronic address: huangshiqing@ruc.edu.cn.
Jian WuState Key Laboratory of Green Pesticide, Guizhou University, Guiyang 550025, China. Electronic address: jwu6@gzu.edu.cn.
Yonggui Robin ChiState Key Laboratory of Green Pesticide, Guizhou University, Guiyang 550025, China; School of Chemistry, Chemical Engineering, and Biotechnology, Nanyang Technological University, Singapore 637371 Singapore. Electronic address: robinchi@ntu.edu.sg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionQuinazolin-4-one is a privileged scaffold in drugs with broad clinical applications. Conventionally, an o-amino group was generally needed to be pre-installed on the benzoic acid-derived starting materials for the efficient condensation reactions towards quinazolin-4-ones. The application of benzene derivatives without requisite amino and / or carbonyl groups as the quinazolin-4-one starting materials has not been disclosed. Therefore, we report herein the fabrication of NHC molecules with nitrobenzenes for facile access to quinazolin-4-one derivatives.

objectivesTo develop an unprecedented synthetic method utilizing nitrobenzenes and N-heterocyclic carbene (NHC) molecules, to elucidate the novel reaction mechanism through experimental and computational studies, to synthesize a series of quinazolin-4-one derivatives, and to evaluate their in vitro antibacterial activity.

methodsA synthetic method involving nitrobenzenes and NHC molecules was developed. The novel reaction mechanism was elucidated through isotopic labeling experiments and computational studies, and a series of quinazolin-4-one derivatives were synthesized. The synthesized compounds were evaluated for in vitro antifungal activity against four plant pathogens using the mycelial growth rate method.

resultsWe report for the first time an unprecedented synthetic method involving nitrobenzene and NHC molecules. The nitrobenzene substrate acts as a novel type of NHC acceptor, enabling a condensation reaction with the NHC molecule through a multi-step nucleophilic addition/rearrangement/dehydration cascade process. This conceptually novel reaction mechanism has been thoroughly investigated through experimental and computational studies. A variety of substituents with different electronic properties are tolerated on both the nitrobenzene and NHC reactants. A series of quinazolin-4-one products can be readily accessed using the current synthetic strategy, and they exhibit promising antifungal activity in plant protection.

conclusionWe have developed a conceptually novel incorporation reaction between nitrobenzenes and NHC molecules. Synthesized compound 13 exhibited broad-spectrum antifungal activity, providing a basis for its development potential as a new framework for pesticide design.

Indexed as

Antifungal activityCascade reactionN-heterocyclic carbeneNitrobenzeneQuinazolin-4-one derivatives

Identifiers

PMID41265637
PMCPMC13453963

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