试剂
脱羧
化学
组合化学
烷基化
催化作用
配体(生物化学)
电化学
烷基
光催化
杂原子
有机化学
电极
生物化学
物理化学
受体
作者
Keyong Yuan,Tian Xie,Jia-Bao Wang,Dali Wang,Ming Shan
标识
DOI:10.1002/anie.202500744
摘要
A photoelectrocatalytic method is presented that achieves direct decarboxylative C(sp3)–P coupling, providing a modular route to alkylphosphinates and alkylphosphonates from readily available carboxylic acids. The success of this reaction hinges on the synergistic combination of electrochemical anodic oxidation and photocatalytic ligand to metal charge transfer (LMCT) decarboxylation. By employing P(III) reagents as limiting reagents, our approach enables efficient alkyl modification of medicinally important nucleosides and complex molecules derived phosphonites, which were challenging to access by existing methods. Detailed mechanistic studies elucidate the critical roles of Fe catalysts and additives, offering valuable insights into the reaction pathway and laying the foundation for future advancements in photoelectrocatalytic C(sp3)–heteroatom bond‐forming reactions.
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