Cu(I)-Catalyzed [3 + 3] Cycloaddition Reaction of Ethynyl Methylene Cyclic Carbamates and Azomethine Imines: Synthesis of 1,2,4-Triazinane Derivatives

A copper-catalyzed, efficient, operationally simple, and general method for straightforward synthesis of 1,2,4-triazinane derivatives employing EMCCs (ethynyl methylene cyclic carbamates) as precursors reacting with azomethine imines was first reported. A wide variety of 1,2,4-triazinane derivatives were obtained in acceptable to good yields under mild conditions. This protocol features a broad substrate scope, high functional group tolerance, and easy operation, therefore enabling late-stage functionalization. In addition, a scale-up experiment further highlighted the synthetic utility.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-09-18
DOI
https://doi.org/10.1021/acs.joc.5c00939
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Cu(I)-Catalyzed [3 + 3] Cycloaddition Reaction of Ethynyl Methylene Cyclic Carbamates and Azomethine Imines: Synthesis of 1,2,4-Triazinane Derivatives

Xiang Ji, Xiaoting Xie, Shiwu Li, Zhifei Zhao
1 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.94
article

Cu(I)-Catalyzed [3 + 3] Cycloaddition Reaction of Ethynyl Methylene Cyclic Carbamates and Azomethine Imines: Synthesis of 1,2,4-Triazinane Derivatives

Xiang Ji, Xiaoting Xie, Shiwu Li, Zhifei Zhao
article en
1 citations

Abstract

A copper-catalyzed, efficient, operationally simple, and general method for straightforward synthesis of 1,2,4-triazinane derivatives employing EMCCs (ethynyl methylene cyclic carbamates) as precursors reacting with azomethine imines was first reported. A wide variety of 1,2,4-triazinane derivatives were obtained in acceptable to good yields under mild conditions. This protocol features a broad substrate scope, high functional group tolerance, and easy operation, therefore enabling late-stage functionalization. In addition, a scale-up experiment further highlighted the synthetic utility.

The Journal of Organic ChemistryVol. 90(38)
Shihezi University (CN)
Openalex Percentile: Top 21%
Catalytic C–H Functionalization Methods
0.94
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