硫
化学
薗头偶联反应
芳基
催化作用
电泳剂
三氟甲磺酸
选择性
组合化学
偶联反应
炔基化
盐(化学)
有机化学
钯
烷基
作者
Lei Liang,Hong‐Ying Niu,Renlong Li,Yao-Fei Wang,Jin-Kai Yan,Chang-Gong Li,Hai‐Ming Guo
出处
期刊:Organic Letters
[American Chemical Society]
日期:2020-08-18
卷期号:22 (17): 6842-6846
被引量:51
标识
DOI:10.1021/acs.orglett.0c02364
摘要
The classical Sonogashira reaction of aryl electrophiles in the presence of Pd catalysts has been well established as a potent method for arylalkyne synthesis. However, the site-selective C(sp2)-C(sp) cross-coupling strategy using a non-noble-metal catalyst is rare. An efficient alternative approach for the synthesis of arylalkynes via a Cu-catalyzed Sonogashira-type reaction promoted by visible light is described. This method enables site-selective alkynylation from aryl sulfonium salts derived from diverse arenes to a set of arylalkynes with high selectivity and high functional-group compatibility. Moreover, rapid alkynylation of drug molecules is demonstrated.
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