Abstract

AbstractThe first continuous flow syntheses of amido and thiolato families are reported. Our studies focused on [M(NHC)(Cbz)] (Cbz=carbazolyl) and [M(NHC)(SPh)] (NHC=N‐heterocyclic carbene) as general proof‐of‐concepts and has led to a simple protocol with unprecedented short reaction times and high product yields. The scope of supporting ligands and substrates permits to assess the versatility of the process and a one‐pot synthesis starting from the imidazolium salt, metal source and carbazole substrate highlights the simplicity and sustainability of this operating design. The process was made possible through a detailed mechanistic understanding of the underlying reaction chemistry.

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