Department of Chemistry, University of Turin, Via P. Giuria 7, 10125 Turin, Italy.
Department of Drug Science and Technology and NIS - Centre for Nanostructured Interfaces and Surfaces, University of Turin, Via P. Giuria 9, 10125 Turin, Italy.
Molecules. 2019 Jan 14;24(2):288. doi: 10.3390/molecules24020288.
Transition-metal mediated C⁻H bond activation and functionalization is one of the most straightforward and powerful tools in modern organic synthetic chemistry. Oxidative C⁻H/C⁻H coupling reactions between two (hetero)arenes under heterogeneous catalysis may be a valuable means for the production of a plethora of bi(hetero)aryls, and one that adheres to the increasing demand for atom-economic and sustainable chemistry. We have therefore developed a reusable heterogeneous catalytic system, which is based on Pd cross-linked β-cyclodextrin, to perform an efficient microwave-assisted oxidative C⁻H/C⁻H cross coupling process between benzothiazoles and methyl thiophene in the presence of green solvents.
过渡金属介导的 C-H 键活化和功能化是现代有机合成化学中最直接、最强大的工具之一。在多相催化下,两种(杂)芳环之间的氧化 C-H/C-H 偶联反应可能是生产大量双(杂)芳基的一种有价值的方法,这符合对原子经济性和可持续化学的日益增长的需求。因此,我们开发了一种基于钯交联β-环糊精的可重复使用的多相催化体系,以在绿色溶剂存在下,在微波辅助下实现苯并噻唑和甲基噻吩之间的高效氧化 C-H/C-H 交叉偶联过程。