Cu(I)催化的[3 + 3]环加成反应:1,2,4-三嗪烷衍生物的合成

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Xiaoting Xie, , , Xiang Ji, , , Zhifei Zhao*, , and , Shi-Wu Li*, 
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引用次数: 0

摘要

首次报道了一种铜催化、高效、操作简单、直接合成1,2,4-三嗪烷衍生物的方法,该方法采用emcc(乙基亚甲基环氨基甲酸酯)作为前驱体与亚甲亚胺反应。在温和的条件下,以可接受的收率得到了各种各样的1,2,4-三嗪烷衍生物。该协议具有广泛的基板范围,高官能团容忍度和易于操作,因此可以实现后期功能化。此外,一个放大实验进一步突出了合成效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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