Universität Rostock, Institut für Chemie, Albert-Einstein-Str. 3a, 18059 Rostock, Germany.
Org Biomol Chem. 2020 Aug 26;18(33):6531-6536. doi: 10.1039/d0ob01194k.
Several thieno[2,3-h]-/[3,2-h]- and [2,3-f]quinolines have been synthesised from 2,3-dihalogenated pyridines or -quinolines by site-selective Pd catalysed cross-coupling reactions and Brønsted acid mediated cycloisomerisations as the final key step. This newly developed synthetic strategy is used in a modular way to synthesize diverse regioisomeric derivatives, tolerates various functional groups, and proceeds with high selectivity, and the desired final products have been isolated in high overall yields.
几种噻吩并[2,3-h]-/[3,2-h]-和[2,3-f]喹啉已经通过 2,3-二卤代吡啶或喹啉的选择性 Pd 催化交叉偶联反应和布朗斯台德酸介导的环化异构化作为最后关键步骤来合成。这种新开发的合成策略以模块化的方式用于合成各种区域异构体衍生物,可耐受各种官能团,具有高选择性,所需的最终产物以高总收率分离出来。