化学
反应性(心理学)
区域选择性
催化作用
钯
溶剂
偶联反应
反应条件
组合化学
氧化磷酸化
反应机理
联轴节(管道)
功能群
有机化学
医学
机械工程
生物化学
聚合物
替代医学
病理
工程类
出处
期刊:Organic Letters
[American Chemical Society]
日期:2015-08-31
卷期号:17 (18): 4456-4459
被引量:55
标识
DOI:10.1021/acs.orglett.5b02115
摘要
An unprecedented weak coordination promoted dehydrogenative cross-coupling reaction has been developed by palladium catalysis, which provides a convenient access to a wide range of 2,2′-difunctional biaryls from easily accessible substrates. Both HFIP solvent and oxidants serve as the critical factors in this new reaction. A plausible mechanism involving Pd(II)/Pd(IV) is proposed. The reaction demonstrates excellent reactivity, broad functional-group tolerance and high yields.
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