化学
部分
芳基
酰胺
催化作用
醛
配体(生物化学)
取代基
乙醚
药物化学
反应性(心理学)
镍
组合化学
炔烃
三键
炔基化
有机化学
双键
烷基
替代医学
受体
病理
医学
生物化学
作者
Jun Yi,Yang Li,Chungu Xia,Fuwei Li
标识
DOI:10.1021/acs.joc.5b00669
摘要
An efficient nickel catalyst system for the direct ortho C-H alkynylation of the amides has been successfully developed with the directing assistance of 8-aminoquinoline. It was found that the flexible bis(2-dimethylaminoethyl) ether (BDMAE) ligand was critical to achieve the optimized reactivity. This protocol showed good tolerance toward not only a wide range of (hetero)aryl amides but also the rarely studied α,β-unsaturated alkenyl amide. The directing amide group could be easily transformed to aldehyde or ester in high yields. Meanwhile, the removable TIPS substituent on the resultant aryl/alkenyl alkynes could be further converted to an aryl moiety through a Sila-Sonogashira coupling reaction. This Ni-catalyzed alkynylation procedure provides an alternative approach to construct a C(sp(2))-C(sp) bond.
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