Merging Photoinduced Iron-Catalyzed Decarboxylation with Copper Catalysis for C–N and C–C Couplings
Citations Over TimeTop 1% of 2023 papers
Abstract
We report a photoinduced iron/copper dual-catalytic strategy for the radical decarboxylation functionalization of aliphatic carboxylic acids. The photoinduced ligand-to-iron charge transfer process under light was initially occurred to generate an unstabilized alkyl radical, and the copper catalyst delivered the radical and enabled the subsequent coupling reactions to form C–N or C–C bonds. By merging iron-catalyzed decarboxylation with copper catalysis, this system allows the smooth conversion of a wide range of aliphatic carboxylic acids for the amination, decarboxylative dehydrogenation, and alkylation efficiently. A wide variety of complex drug or natural molecules is applicable, suggesting that this strategy would facilitate rapid compound library synthesis and benefit to the discovery of pharmaceutical agents.
Related Papers
- → In situ X-ray diffraction study of dehydrogenation of MgH2 with Ti-based additives(2014)34 cited
- → A kinetics study on continuous dehydrogenation of dodecahydro‐N‐ethylcarbazole(2024)4 cited
- → The catalytic effect of ZrCl4 on thermal dehydrogenation LiAlD4(2020)4 cited
- → Synthesis of Zn2TiO4 via solid-state method as a promising additive for dehydrogenation properties of NaAlH4(2023)3 cited
- → Dehydrogenation – Biological(2002)