Clerc Arnaud, Marelli Enrico, Adet Nicolas, Monot Julien, Martín-Vaca Blanca, Bourissou Didier
Laboratoire Hétérochimie Fondamentale et Appliquée (UMR 5069), Université de Toulouse (UPS), CNRS 118 route de Narbonne F-31062 Toulouse France
Chem Sci. 2020 Oct 30;12(1):435-441. doi: 10.1039/d0sc05036a.
An original multi-cooperative catalytic approach was developed by combining metal-ligand cooperation and Lewis acid activation. The [(SCS)Pd] complex featuring a non-innocent indenediide-based ligand was found to be a very efficient and versatile catalyst for the Conia-ene reaction, when associated with Mg(OTf). The reaction operates at low catalytic loadings under mild conditions with HFIP as a co-solvent. It works with a variety of substrates, including those bearing internal alkynes. It displays complete 5- 6- regio-selectivity. In addition, except for the highly congested Bu-substituent, the reaction occurs with high stereo-selectivity, making it synthetically useful and complementary to known catalysts.
通过结合金属-配体协同作用和路易斯酸活化,开发了一种原创的多协同催化方法。发现具有非惰性茚二亚胺基配体的[(SCS)Pd]配合物与Mg(OTf)结合时,是用于柯尼亚-烯反应的非常高效且通用的催化剂。该反应在温和条件下以低催化负载量进行,以HFIP作为共溶剂。它适用于多种底物,包括带有内炔的底物。它表现出完全的5-6区域选择性。此外,除了高度拥挤的叔丁基取代基外,该反应具有高立体选择性,使其在合成上有用且可补充已知催化剂。