Manganese-catalyzed Sonogashira coupling of aryl iodides

被引：12
作者：
Qi, Xinxin [1 ]
Jiang, Li-Bing [1 ]
Wu, Xiao-Feng [1 ,2 ]
机构：
[1] Zhejiang Sci Tech Univ, Dept Chem, Xiasha Campus, Hangzhou 310018, Zhejiang, Peoples R China
[2] Univ Rostock, Leibniz Inst Katalyse eV, Albert Einstein Str 29a, D-18059 Rostock, Germany
来源：
TETRAHEDRON LETTERS | 2016年 / 57卷 / 15期
关键词：
Manganese; Sonogashira coupling; Aryl iodides; Cross coupling; Nanoparticles; IRON/COPPER COCATALYZED ALKYNYLATION; CARBON BOND FORMATION; HETEROARYL HALIDES; TERMINAL ALKYNES; PALLADIUM; EFFICIENT; HYDROGEN; SYSTEM; PEG;
D O I：
10.1016/j.tetlet.2016.03.014
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
An interesting manganese-catalyzed Sonogashira coupling reaction of aryl iodides has been developed. With PEG-400 as the green solvent and under mild reaction conditions, a variety of diarylacetylenes were obtained in moderate to good yields. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码：1706 / 1710
页数：5
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