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Copper‐Catalyzed Radical Cross‐Coupling of Redox‐Active Oxime Esters, Styrenes, and Boronic Acids
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2018-10-19 , DOI: 10.1002/anie.201809820
Xiao‐Ye Yu 1 , Quan‐Qing Zhao 1 , Jun Chen 1 , Jia‐Rong Chen 1 , Wen‐Jing Xiao 1, 2
Affiliation  

A visible‐light‐driven, copper‐catalyzed three‐component radical cross‐coupling of oxime esters, styrenes, and boronic acids has been developed. Key steps of this protocol involve catalytic generation of an iminyl radical from a redox‐active oxime ester and subsequent C−C bond cleavage to generate a cyanoalkyl radical. Upon its addition to styrene, the newly formed benzylic radical undergoes coupling with a boronic‐acid‐derived ArCuII complex to achieve 1,1‐diarylmethane‐containing alkylnitriles.

中文翻译:

铜催化的氧化还原活性肟酯,苯乙烯和硼酸的自由基交叉偶联

已经开发了一种由可见光驱动,铜催化的肟酯,苯乙烯和硼酸的三组分自由基交叉偶联反应。该协议的关键步骤涉及从氧化还原活性肟酯催化生成亚胺基,然后进行C-C键裂解,生成氰基烷基。在将其添加到苯乙烯中后,新形成的苄基与硼酸衍生的ArCu II配合物偶联,从而获得含1,1-二芳基甲烷的烷基腈。
更新日期:2018-10-19
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