Olu-Igbiloba Oluwaseun A, Sitzmann Helmut, Manolikakes Georg
Department of Chemistry, RPTU Kaiserslautern-Landau, D-67663 Kaiserslautern, Germany.
J Org Chem. 2024 May 17;89(10):6903-6914. doi: 10.1021/acs.joc.4c00271. Epub 2024 May 3.
A three-component synthesis of α-substituted -sulfonyl amines from aryl aldehydes, primary sulfonamides, and (hetero)arenes is described. This transformation enables a straightforward and modular synthesis of highly substituted sulfonamide scaffolds in good yields. The direct functionalization of C(sp)-H bonds via cobalt-catalyzed C-H-activation offers an appealing and atom-economical alternative to classical methods for the synthesis of α-arylated amines such as the Petasis or Mannich-type reactions.
本文描述了一种由芳醛、伯磺酰胺和(杂)芳烃合成α-取代磺酰基胺的三组分反应。该转化反应能够以良好的产率直接且模块化地合成高度取代的磺酰胺骨架。通过钴催化的C-H活化实现C(sp)-H键的直接官能团化,为合成α-芳基胺的经典方法(如Petasis反应或曼尼希型反应)提供了一种有吸引力且原子经济的替代方法。