催化作用
偶氮
氧化还原
化学
联氨(抗抑郁剂)
选择性催化还原
羟胺
过渡金属
药物化学
组合化学
无机化学
有机化学
色谱法
作者
Zhuchunguang Liu,Xiaojian Li,Zhijun Wang,Huan Mu,Bo Xiao,Weichao Xue,Jiliang Zhou,Zhaowen Dong
标识
DOI:10.1002/anie.202515638
摘要
Abstract While homogeneous catalysis remains predominantly dominated by transition metal complexes, the utilization of main group compounds as redox catalysts for diverse chemical transformations represents a long‐sought yet underexplored frontier. This work reports the catalytic reduction of N 2 O in the presence of HBpin via an unprecedented E II /E IV O (E = Ge, Sn) redox platform, employing carbodiphosphorane ligated germylene or stannylene as the catalyst. The key Ge IV and Sn IV ‐oxo intermediates have been isolated and characterized. Furthermore, we extend this redox platform to achieve efficient and chemodivergent reduction of nitroarenes under mild conditions. Notably, through systematic modulation of reaction conditions, four different reduced products including amino, hydroxylamine, azoxy, and hydrazine derivatives can be synthesized from nitroarenes with high yields and selectivity. This work establishes a novel heavy group 14 element‐based catalytic manifold and unlocks new opportunities for the application of heavy carbene analogues in redox catalysis.
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