Institute for Organic and Biomolecular Chemistry, Georg-August-Universität Göttingen, Tammannstr. 2, 37077 Göttingen, Germany.
Chem Commun (Camb). 2018 Nov 13;54(91):12879-12882. doi: 10.1039/c8cc07732k.
Electrooxidative peri-C-H activation was accomplished by versatile ruthenium(ii) catalysis in terms of C-H/N-H and C-H/O-H functionalization. Thus, alkyne annulations proved viable with ample scope by organometallic C-H activation. The sustainable electrocatalysis exploited electricity, thereby avoiding the use of toxic transition metals as sacrificial oxidants. The robust ruthenium(ii)-electrocatalysis was operative in a protic alcohol/H2O reaction medium with excellent levels of position-, regio- and chemo-selectivity.
通过多功能钌(ii)催化实现了电化学邻位 C-H 键活化,用于 C-H/N-H 和 C-H/O-H 官能化。因此,通过金属有机 C-H 活化实现了广泛的炔烃环化反应。可持续的电催化利用了电能,从而避免了使用有毒的过渡金属作为牺牲氧化剂。在质子醇/H2O 反应介质中,稳健的钌(ii)电催化具有优异的位置、区域和化学选择性。