A General Copper-based Photoredox Catalyst for Organic Synthesis: Scope, Application in Natural Product Synthesis and Mechanistic Insights

Authors

  • Christopher Deldaele Laboratoire de Chimie Organique Service de Chimie et PhysicoChimie Organiques Université libre de Bruxelles (ULB) Avenue F. D. Roosevelt 50, CP160/06, 1050 Brussels, Belgium
  • Bastien Michelet Laboratoire de Chimie Organique Service de Chimie et PhysicoChimie Organiques Université libre de Bruxelles (ULB) Avenue F. D. Roosevelt 50, CP160/06, 1050 Brussels, Belgium
  • Hajar Baguia Laboratoire de Chimie Organique Service de Chimie et PhysicoChimie Organiques Université libre de Bruxelles (ULB) Avenue F. D. Roosevelt 50, CP160/06, 1050 Brussels, Belgium
  • Sofia Kajouj Laboratoire de Chimie Organique Service de Chimie et PhysicoChimie Organiques Université libre de Bruxelles (ULB) Avenue F. D. Roosevelt 50, CP160/06, 1050 Brussels, Belgium
  • Eugenie Romero Laboratoire de Chimie Organique Service de Chimie et PhysicoChimie Organiques Université libre de Bruxelles (ULB) Avenue F. D. Roosevelt 50, CP160/06, 1050 Brussels, Belgium
  • Cecile Moucheron Laboratoire de Chimie Organique et Photochimie Service de Chimie et PhysicoChimie Organiques Université libre de Bruxelles (ULB) Avenue F. D. Roosevelt 50, CP160/08, 1050 Brussels, Belgium
  • Gwilherm Evano Laboratoire de Chimie Organique Service de Chimie et PhysicoChimie Organiques Université libre de Bruxelles (ULB) Avenue F. D. Roosevelt 50, CP160/06, 1050 Brussels, Belgium;, Email: gevano@ulb.ac.be

DOI:

https://doi.org/10.2533/chimia.2018.621

Keywords:

Copper(0), Copper catalysis, Natural products, Photoredox catalysis, Radicals

Abstract

Organic transformations can broadly be classified into four categories including cationic, anionic, pericyclic and radical reactions. While the last category has been known for decades to provide remarkably efficient synthetic pathways, it has long been hampered by the need for toxic reagents, which considerably limited its impact on chemical synthesis. This situation has come to an end with the introduction of new concepts for the generation of radical species, photoredox catalysis – which simply relies on the use of a catalyst that can be activated upon visible light irradiation – certainly being the most efficient one. The state-of-the-art catalysts mostly rely on the use of ruthenium and iridium complexes and organic dyes, which still considerably limits their broad implementation in chemical processes: alternative readily available catalysts based on inexpensive, environmentally benign base metals are therefore strongly needed. Furthermore, expanding the toolbox of methods based on photoredox catalysis will facilitate the discovery of new light-mediated transformations. This article details the use of a simple copper complex which, upon activation with blue light, can initiate a broad range of radical reactions.

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Published

2018-09-01

How to Cite

[1]
C. Deldaele, B. Michelet, H. Baguia, S. Kajouj, E. Romero, C. Moucheron, G. Evano, Chimia 2018, 72, 621, DOI: 10.2533/chimia.2018.621.