摘要
A method for the catalytic alpha-arylation of indolin-3-ones was developed. The catalytic system comprising Pd(dba)(2) and PAd(3) was found to be optimal for the transformation. The protocol features broad functional group compatibility in that a range of arylated indoxyl derivatives bearing a fully substituted carbon center was synthesized with high efficiency. A preliminary bioassay study revealed that the selected indole-substituted indolin-3-ones exhibit favorable cytotoxic activities against HCT-116 cancer cell line.
原文 | English |
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頁(從 - 到) | 4660-4663 |
頁數 | 4 |
期刊 | Chemical Communications |
卷 | 56 |
發行號 | 34 |
DOIs | |
出版狀態 | Published - 30 4月 2020 |