Copper-catalyzed allenynylative C-P coupling of diynylic acetates with hydrophosphoryl compounds leading to phosphorylated allenynes

被引:1
|
作者
Liu, Shaoqing [1 ]
Yin, Kaixin [1 ]
Fan, Yishuai [1 ]
Han, Li-Biao [2 ,3 ]
Shen, Ruwei [1 ]
机构
[1] Nanjing Tech Univ, Coll Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China
[2] Shaoxing Univ, Coll Chem & Chem Engn, Res Ctr Adv Catalyt Mat & Funct Mol Synth, Shaoxing 312000, Peoples R China
[3] Zhejiang Yangfan New Mat Co Ltd, Shangyu 312369, Zhejiang, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2024年 / 11卷 / 17期
基金
中国国家自然科学基金;
关键词
ENANTIOSELECTIVE PROPARGYLIC AMINATION; BETA-KETOESTERS; ESTERS; CYCLOADDITION; CARBONATES; ALCOHOLS; AMINES;
D O I
10.1039/d4qo01021c
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A highly efficient copper-catalyzed coupling reaction of diynylic acetates with hydrophosphoryl compounds is developed based on the concept of site-selective nucleophilic interception of copper-cumulenylidene-type intermediates. This reaction enables an expeditious synthesis of a novel class of conjugated allenynylphosphoryl compounds in good to high yields from readily available materials under mild conditions. A copper-catalyzed allenynylative C-P coupling reaction between diynylic acetates and hydrophosphoryl compounds is developed via nucleophilic interception of copper-cumulenylidene intermediates.
引用
收藏
页码:4836 / 4841
页数:6
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