化学
钯
催化作用
还原消去
选择性
转化(遗传学)
组合化学
活化能
立体化学
光化学
药物化学
物理化学
有机化学
生物化学
基因
作者
Joy M. Racowski,Nicholas D. Ball,Melanie S. Sanford
摘要
This communication describes the first observation and study of C–H activation at a PdIV center. This transformation was achieved by designing model complexes in which the rate of reductive elimination is slowed relative to that of the desired C–H activation process. Remarkably, the C–H activation reaction can proceed under mild conditions and with complementary site selectivity to analogous transformations at PdII. These results provide a platform for incorporating this new reaction as a step in catalytic processes.
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