Copper-Mediated Coupling of 1,1-Dibromo-1-alkenes with Nitrogen Nucleophiles: A General Method for the Synthesis of Ynamides

被引:204
作者
Coste, Alexis [1 ]
Karthikeyan, Ganesan [1 ]
Couty, Francois [1 ]
Evano, Gwilherm [1 ]
机构
[1] Univ Versailles St Quentin Yvelines, Inst Lavoisier Versailles, CNRS, UMR 8180, F-78035 Versailles, France
关键词
copper; cross-coupling; dibromoalkenes; homogeneous catalysis; ynamides; RING-CLOSING METATHESIS; N-FUNCTIONALIZED; 1-ALKYNYLAMIDES; AXIALLY CHIRAL ANILIDES; INTRAMOLECULAR AMIDATION; CATALYZED CYCLIZATION; ALKYNYL BROMIDES; DERIVATIVES; 1,6-DIYNES; CYCLOADDITIONS; CHEMISTRY;
D O I
10.1002/anie.200901099
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mild reaction conditions are the advantage of the title reaction, which allows straightforward entry to a variety of ynamides starting from readily available 1,1-dibromo-1- alkenes, which act as attractive alkynylating agents (see scheme; EWG=electron-withdrawing group, DMF=N,Ndimethylformamide). © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:4381 / 4385
页数:5
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