氰化
钯
芳基
化学
催化作用
氰化物
试剂
卤化物
溴苯
溴化物
卤代芳基
有机化学
高分子化学
药物化学
无机化学
烷基
作者
Mark Sundermeier,Alexander John Zapf,Matthias Beller
标识
DOI:10.1002/anie.200250778
摘要
A useful source of cyanide for the palladium-catalyzed cyanation of aryl halides is acetone cyanohydrin (see scheme; dpppe=1,5-bis(diphenylphosphanyl)pentane, tmeda=N,N,N′,N′-tetramethylethylenediamine). The key to the success of the reaction is the slow dosage of the cyanation reagent to the reaction mixture to prevent the deactivation of the palladium catalyst caused by excess cyanide ions in solution.
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