Abstract
AbstractThe synthesis of a bis‐silylated (NHC)AuCl (NHC=N‐heterocyclic carbene) complex and the formation of a hybrid silica material by the sol–gel process by cogelification with tetraethylorthosilicate under fluoride catalysis are described. This material was characterized by using 29Si solid‐state NMR spectroscopy, N2 sorption measurements, electron microscopy, and elemental analysis. It was tested as a reusable catalyst in the rearrangement of allylic esters in conjunction with a silver salt under microwave conditions and it displayed a much better performance than a homogeneous analogue. This catalyst is active and recyclable in the cycloisomerization of γ‐alkynoic acids to five‐membered enol‐lactones at room temperature in two reaction media, a toluene/water biphasic system and a deep eutectic solvent.
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