化学
氰化
磷化氢
亲核细胞
光催化
烷基
组合化学
自由基离子
氧化加成
催化作用
亲核加成
光化学
有机化学
光催化
离子
作者
Jing Li,Yanyan Zhang,Shengqing Zhu,Lingling Chu
标识
DOI:10.1002/chem.202501154
摘要
While notable progress has been made in alkene cyanation for the synthesis of alkyl nitriles, catalytic strategies enabling the direct dicyanation of simple alkenes remain relatively under-explored. In this study, we introduce a synergistic phosphine-photoredox catalytic system that facilitates the direct dicyanation of styrenes using TMSCN in the presence of oxidant. This approach utilizes a phosphorus radical cation to initiate an oxidative radical-polar crossover with alkenes, followed by sequential nucleophilic cyanation. This protocol allows for the efficient synthesis of alkyl 1,2-dinitriles from alkenes under mild conditions. Notably, the method exhibits broad substrate scope and commendable efficiency, serving as a valuable complement to existing cyanation methodologies. The synthetic utility of the dinitrile products is further demonstrated through diverse derivatization reactions, highlighting their applicability in constructing nitrogen-rich molecular architectures. Mechanistic studies provide further insight into the reaction pathway and underscore the potential of phosphorus radical cations in alkene functionalization.
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