Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, D-45470 Mülheim an der Ruhr, Germany.
Org Lett. 2020 Jul 17;22(14):5671-5674. doi: 10.1021/acs.orglett.0c02067. Epub 2020 Jul 8.
We report a nucleophilic substitution reaction of five-membered hetarylsulfonium salts that results in a change of the substitution pattern on the arene. The products of these -substitutions are hard to access synthetically otherwise. The sulfonium salts that serve as starting materials are generated by a highly site-selective C-H functionalization reaction.
我们报告了五元杂芳基锍盐的亲核取代反应,该反应导致芳环上的取代模式发生变化。否则,这些 -取代产物很难通过合成获得。用作起始材料的锍盐是通过高度选择性的 C-H 功能化反应生成的。