化学
立体中心
钴
催化作用
烷基
位阻效应
芳基
反应性(心理学)
配体(生物化学)
试剂
Negishi偶联反应
组合化学
催化循环
选择性
有机化学
药物化学
对映选择合成
受体
医学
生物化学
替代医学
病理
作者
Jingyi Wang,Xuzhong Shen,Chen Xu,Yinwei Bao,Jian He,Zhan Lu
摘要
Cobalt-catalyzed enantioconvergent cross-coupling of α-bromoketones with aryl zinc reagents is achieved to access chiral ketones bearing α-tertiary stereogenic centers with high enantioselectivities. The more challenging and sterically hindered α-bromoketones bearing a 2-fluorophenyl group or β-secondary and tertiary alkyl chains could also be well-tolerated. Adjusting the electronic effect of chiral unsymmetric N,N,N-tridentate ligands is critical for improving the reactivity and selectivity of this transformation, which is beneficial for further studies of asymmetric 3d metal catalysis via ligand modification. The control experiments and kinetic studies illustrated that the reaction involved radical intermediates and the reductive elimination was a rate-determining step.
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