化学
烷基
芳基
羰基化
金属转移
酮
产量(工程)
钯
有机化学
偶联反应
药物化学
催化作用
一氧化碳
冶金
材料科学
作者
Shuhei Sumino,Takahito Ui,Ilhyong Ryu
出处
期刊:Organic Letters
[American Chemical Society]
日期:2013-06-03
卷期号:15 (12): 3142-3145
被引量:73
摘要
Alkyl aryl ketones were synthesized by the carbonylative cross-coupling reaction of alkyl iodides and arylboronic acids under combined Pd/light conditions. In this reaction, it is likely that an acylpalladium species would be formed via carbonylation of the alkyl radical, which would then undergo transmetalation of an arylboronic acid to give the corresponding acyl(aryl)palladium species, ready to undergo reductive elimination to yield the alkyl aryl ketone.
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