Synthesis of conjugated multi-ynamides by copper-catalyzed reactions

被引：8
|
作者：
Betou, Marie [1 ]
Sallustrau, Antoine [1 ]
Toupet, Loic [2 ]
Trolez, Yann [1 ]
机构：
[1] Ecole Natl Super Chim Rennes, CNRS, UMR 6226, F-35708 Rennes 7, France
[2] Univ Rennes 1, CNRS, Inst Phys Rennes, UMR 6251, Rennes, France
来源：
TETRAHEDRON LETTERS | 2015年 / 56卷 / 31期
关键词：
Ynamide; Copper-catalysis; Biphenyl; Thiophene; Triphenylamine; N-FUNCTIONALIZED; 1-ALKYNYLAMIDES; GENERAL-METHOD; OXIDATIVE AMIDATION; EFFICIENT SYNTHESIS; TERMINAL ALKYNES; CYCLOADDITIONS; ALKYNYLATION; 1,1-DIBROMO-1-ALKENES; DERIVATIVES; FORMAMIDES;
D O I：
10.1016/j.tetlet.2015.06.027
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The synthesis of multi-ynamides according to the copper-catalyzed Evano's and Hsung's methods is described. In these new compounds, the ynamide functions are conjugated to each other with a phenyl, a biphenyl, a thienyl, or a triphenylamine spacer. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码：4627 / 4630
页数：4
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