化学选择性
化学
区域选择性
磺酰
催化作用
组合化学
SN2反应
酮
药效团
基质(水族馆)
串联
有机化学
立体化学
烷基
海洋学
材料科学
复合材料
地质学
作者
Jian Ji,Zongjing Hu,Cong Guan,Jinhua Liu,Yaqi Deng,Xuwen Chen,Shunying Liu
标识
DOI:10.1021/acssuschemeng.3c04487
摘要
The first efficient example of the 1,2-carbotriazolization of alkenes with N-sulfonyl-1,2,3-triazoles and aldehydes was developed as an appealing strategy for producing β-triazolized ketones via a copper-catalyzed radical relay process. The products were constructed in one pot with high regioselectivity and chemoselectivity as well as a wide range of substrate scopes, including aromatic and aliphatic aldehydes and alcohols. Preliminary mechanistic study indicates that the reaction proceeds via an SN2-like tandem radical relay desulfonation process. The resulting β-triazolized ketone scaffold shows a good and selective inhibitory activity on osteosarcoma (OS) cell lines at 10 μM, which is promising for use as an efficient pharmacophore for drug discovery.
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