通过铜催化交叉偶联轻松合成二磷酰乙炔

IF 1.5 4区 化学 Q3 CHEMISTRY, ORGANIC Tetrahedron Letters Pub Date : 2024-08-06 DOI:10.1016/j.tetlet.2024.155240
Bowen Fang , Xiaoling Hong , Yage Xue , Yuting Yang , Huilin Li
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引用次数: 0

摘要

含有 1,2-二膦酸分子的有机分子在有机合成中具有重要价值。二磷基乙炔(或称为乙炔-1,2-二基二膦酸盐)是一类用于合成多种磷化合物的分子,适用于多个领域。然而,目前制备二磷基乙炔的化学计量方法通常需要多个步骤或苛刻的条件。在此,我们报告了一种二磷基乙炔的简便合成方法,在这种方法中,现成的乙炔基膦酸盐通过廉价的铜催化与二烷基膦酸盐偶联。以对称或不对称方式轻松制备了一系列二磷基乙炔。该方法具有反应条件温和、无惰性气氛、催化剂廉价、无碱、高效等优点,是合成二磷基乙炔的实用方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Facile synthesis of diphosphoryl acetylenes through copper-catalyzed cross coupling

Organic molecules containing 1,2-diphosphonate moiety are of great value in organic synthesis. Diphosphoryl acetylenes (or named as ethyne-1,2-diyldiphosphonates) are a class of molecules utilized for synthesis of diverse phosphorus compounds applicable in multiple fields. However, present stoichiometric methods for the preparation of diphosphoryl acetylenes generally requires multiple steps or harsh conditions. Herein, we report a facile synthesis of diphosphoryl acetylenes, in which the readily available ethynyl phosphonates couple with dialkyl phosphonates through cheap copper catalysis. A series of diphosphoryl acetylenes in symmetric or unsymmetric fashions are facilely prepared. This protocol demonstrates advantages of mild reaction conditions, inert atmosphere-free, cheap catalyst, base-free, and high efficiency to serve as a practical method for synthesis of diphosphoryl acetylenes.

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来源期刊
Tetrahedron Letters
Tetrahedron Letters 化学-有机化学
CiteScore
3.50
自引率
5.60%
发文量
521
审稿时长
28 days
期刊介绍: Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.
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