化学
芳基
产量(工程)
酮
钯
催化作用
有机化学
反应条件
组合化学
烷基
材料科学
冶金
作者
Erasmus M. Vogl,Stephen L. Buchwald
摘要
A general protocol for the Pd-catalyzed-arylation of nitroalkanes is described. Substituted aryl bromides as well as aryl chlorides can be coupled efficiently with a variety of nitroalkanes under mild conditions to selectively yield the monoarylated products. This method tolerates a number of functional groups including ketones, esters, and olefins. Notably, the arylation of nitroalkanes can be effected chemoselectively over ketone and ester arylation.
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