摘要
Synthetically versatile anthranils as a bifunctional amino source have been employed for the first time to enable direct amination on unactivated C(sp3)-H bonds of thioamides under Cp∗CoIII catalysis. The excellent site-selectivity on primary C(sp3)-H bonds is observed for a diverse array of thioamides with high functional group tolerance. Further applicability of the products is also highlighted through a series of interesting synthetic elaborations.
源语言 | 英语 |
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页(从-至) | 5519-5522 |
页数 | 4 |
期刊 | Chemical Communications |
卷 | 55 |
期 | 38 |
DOI | |
出版状态 | 已出版 - 2019 |