Department of Chemistry, Mohanlal Sukhadia University, Udaipur 313001, India.
Department of Chemistry, Guru Nanak Dev University, Amritsar 143005, India.
Org Lett. 2019 Sep 6;21(17):6726-6730. doi: 10.1021/acs.orglett.9b02340. Epub 2019 Aug 15.
A metal-free diastereo-/regioselective modular synthetic approach for the synthesis of highly constrained tetrahydroquinoline-fused tetracyclic heterocycles from easily available substrates has been developed. This two-step strategy utilizes an Ugi four-component reaction, followed by the intramolecular spirocarbocyclization and iodination reactions in a single operation. The transformation is mild and operationally simple, which provides architecturally complex polycyclic heterocycles with high diastereoselectivity. Furthermore, the preliminary cytotoxicity screening of selected compounds displayed promising anticancer activity against human cancer cell lines.
已开发出一种无金属的非对映选择性/区域选择性模块化合成方法,用于从易得的底物合成高度受限的四氢喹啉稠合四环杂环化合物。该两步策略利用 Ugi 四组分反应,然后在单个操作中进行分子内环化螺环化和碘化反应。该转化温和且操作简单,可提供具有高非对映选择性的结构复杂的多环杂环化合物。此外,对选定化合物的初步细胞毒性筛选显示出对人癌细胞系具有有希望的抗癌活性。