A Recyclable Rh(III)‐Catalyzed C−H Annulation of <i>N</i>‐Pyrimidinyl Aryl Amines with Cyclic 1,3‐Diones in Water

Abstract Rh(III)‐catalyzed synthesis of N ‐heterocycles via regioselective C−H bond activation is both highly efficient and atom‐economical but often hindered by the use of toxic solvents and limited catalyst recyclability. Herein, we present a recyclable Rh(III)‐catalyzed C−H annulation of N ‐pyrimidinyl aryl amines with cyclic 1,3‐diones in water, affording tetrahydrocarbazole derivatives. The basic aqueous environment amplifies the solubility differences between the substrates and the desired product, thereby promoting efficient C−H activation and subsequent cyclization. This method showcases broad substrate compatibility, eliminates the need for pre‐synthesized iodonium ylides, and features an easy work‐up procedure alongside straightforward catalyst recovery. The Rh(III) catalyst retains its activity for at least five cycles, providing a sustainable and practical strategy for N ‐heterocycle synthesis.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-03-20
DOI
https://doi.org/10.1002/ejoc.202500082
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

A Recyclable Rh(III)‐Catalyzed C−H Annulation of N‐Pyrimidinyl Aryl Amines with Cyclic 1,3‐Diones in Water

Hao Zhou, Yijing Xia, Liangliang Shi, Feng Zhang et al.
1 links
European Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
article

A Recyclable Rh(III)‐Catalyzed C−H Annulation of N‐Pyrimidinyl Aryl Amines with Cyclic 1,3‐Diones in Water

Hao Zhou, Yijing Xia, Liangliang Shi, Feng Zhang, Jun Yang, Xiaobo Yang, Jie Li, Zongli Huo, Yuanrui Chen
article en

Abstract

Abstract Rh(III)‐catalyzed synthesis of N ‐heterocycles via regioselective C−H bond activation is both highly efficient and atom‐economical but often hindered by the use of toxic solvents and limited catalyst recyclability. Herein, we present a recyclable Rh(III)‐catalyzed C−H annulation of N ‐pyrimidinyl aryl amines with cyclic 1,3‐diones in water, affording tetrahydrocarbazole derivatives. The basic aqueous environment amplifies the solubility differences between the substrates and the desired product, thereby promoting efficient C−H activation and subsequent cyclization. This method showcases broad substrate compatibility, eliminates the need for pre‐synthesized iodonium ylides, and features an easy work‐up procedure alongside straightforward catalyst recovery. The Rh(III) catalyst retains its activity for at least five cycles, providing a sustainable and practical strategy for N ‐heterocycle synthesis.

European Journal of Organic ChemistryVol. 28(20)
Nankai University (CN), Shenyang Normal University (CN), Tianjin Institute of Pharmaceutical Research (China) (CN), Lishen (China) (CN)
Openalex Percentile: Top 96%
Catalytic C–H Functionalization Methods
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A Recyclable Rh(III)‐Catalyzed C−H Annulation of <i>N</i>‐Pyrimidinyl Aryl Amines with Cyclic 1,3‐Diones in Water — Hao Zhou, Yijing Xia, et al. · European Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS