Liu Weiping, Cera Gianpiero, Oliveira João C A, Shen Zhigao, Ackermann Lutz
Institut für Organische und Biomolekulare Chemie, Georg-August-Universität, Tammannstraße 2, 37077, Göttingen, Germany.
Chemistry. 2017 Aug 25;23(48):11524-11528. doi: 10.1002/chem.201703191. Epub 2017 Aug 4.
C-H alkylations with challenging β-hydrogen-containing alkyl halides were accomplished with sustainable MnCl as the catalyst under phosphine-ligand-free conditions. The proximity-induced benzamide C-H activation occurred with ample substrate scope through rate-determining C-H metalation, also setting the stage for manganese-catalyzed oxidative C-H methylations.
在无膦配体的条件下,以可持续的氯化锰为催化剂,实现了与具有挑战性的含β-氢卤代烃的C-H烷基化反应。通过速率决定步骤的C-H金属化反应,邻近诱导的苯甲酰胺C-H活化反应具有广泛的底物范围,这也为锰催化的氧化C-H甲基化反应奠定了基础。