Construction of Carbon‐Nitrogen Bond From Addition Reaction of Weak Nucleophilic Nitrogen Atom of Imides With <i>Para</i> ‐Quinone Methides

ABSTRACT An efficient 1,6‐conjugate addition for the construction of C–N bonds from the reaction of para ‐Quinone methides ( p ‐QMs) and the weak nucleophilic nitrogen atom of imides was reported. Studies have shown that trimethylamine (Et 3 N) is an essential catalyst for ensuring the successful completion of this synthesis process. The reaction features a wide range of substrates, simple operation, good group tolerance, and high yields.

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Publication Details

Journal
Journal of Heterocyclic Chemistry
Published
2025-11-27
DOI
https://doi.org/10.1002/jhet.70141
Primary Topic
Synthesis of Indole Derivatives
Type
article
Field-Weighted Citation Impact
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article

Construction of Carbon‐Nitrogen Bond From Addition Reaction of Weak Nucleophilic Nitrogen Atom of Imides With Para ‐Quinone Methides

Liangce Rong, Yi‐Ting Wang, Feixiang Luo, G. L. TONG
Journal of Heterocyclic Chemistry
Synthesis of Indole Derivatives
article

Construction of Carbon‐Nitrogen Bond From Addition Reaction of Weak Nucleophilic Nitrogen Atom of Imides With Para ‐Quinone Methides

Liangce Rong, Yi‐Ting Wang, Feixiang Luo, G. L. TONG
article en

Abstract

ABSTRACT An efficient 1,6‐conjugate addition for the construction of C–N bonds from the reaction of para ‐Quinone methides ( p ‐QMs) and the weak nucleophilic nitrogen atom of imides was reported. Studies have shown that trimethylamine (Et 3 N) is an essential catalyst for ensuring the successful completion of this synthesis process. The reaction features a wide range of substrates, simple operation, good group tolerance, and high yields.

Journal of Heterocyclic ChemistryVol. 63(2)
Jiangsu Normal University (CN), Xuzhou Medical College (CN), Jiangsu Nhwa Pharmaceutical (China) (CN), Second Affiliated Hospital of Xuzhou Medical College (CN)
Openalex Percentile: Top 72%
Synthesis of Indole Derivatives
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