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Indazolin-3-ylidenes (Indy*): easily accessible, sterically-hindered indazole-derived N-heterocyclic carbenes and their application in gold catalysis.

Jin ZhangTing LiuGaopeng ZhangJianglong CaiYue WangJian-Bo TongYangmin MaRoman SzostakMichal Szostak
Published in: Dalton transactions (Cambridge, England : 2003) (2024)
Sterically-hindered N-heterocyclic carbenes (NHCs) with functionalized N -wingtips are a pivotal class of ligands in organic synthesis. Herein, we report the first class of sterically-hindered N-heterocyclic carbenes based on the indazole framework. These ligands combine the strong σ-donation of the carbene center due to the carbene placement at the C3-indazole position with the sterically-hindered and flexible N -substitution with the versatile 2,6-bis(diphenylmethyl)aryl moiety that extends beyond the metal centre for the first time in non-classical N-heterocyclic carbenes. The ligands are readily accessible by the rare Cadogan indazole synthesis of sterically-hindered N -aryl-1-(2-nitrophenyl)methanimines. Steric and electronic characterization as well as catalytic studies in the synthesis of oxazolines are described. Considering the unique properties of indazole-derived carbenes, we anticipate that this class of compounds will find broad application in organic synthesis and catalysis.
Keyphrases
  • mass spectrometry
  • quantum dots
  • ultrasound guided
  • liquid chromatography
  • crystal structure
  • simultaneous determination