化学
钯
区域选择性
烷基
催化作用
芳基
选择性
药物化学
组合化学
金属
有机化学
作者
Irene Martín,Cristina Aragoncillo,Pedro Almendros
标识
DOI:10.1002/adsc.202001267
摘要
Abstract A selective palladium‐catalyzed C( sp ) arylation/carbocyclization/iodonium migration reaction sequence has been accomplished. Novel 2‐iodo‐1‐aryl‐9 H ‐carbazoles are now easily available. As this result is contrary to the selectivity observed using gold catalysis, the formation of 2‐iodocarbazoles is noticeable, suggesting a metal‐controlled cyclization through chemo‐ and regioselective 1,2‐alkyl migration and 1,4‐iodonium migration. magnified image
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