Palladium-Catalyzed Regioselective Coupling Cyclohexenone into Indoles: Atom-Economic Synthesis of β-Indolyl Cyclohexenones and Derivatization Applications.
Zhen-Kang WenXiao-Xue WuWen-Kai BaoJing-Jing XiaoJian-Bin ChaoPublished in: Organic letters (2020)
Herein, we report a palladium-catalyzed dehydrogenative cross-coupling of indoles with cyclic enones to give β-indolyl cyclic enones under mild and neutral reaction conditions. The key to the success is to explore a mild condition, which ensures the indole C-H activation and subsequent syn β-hydride elimination through rapid enolization isomerization of Pd(II)-enolate while suppressing other undesired side reactions. Synthetic utility has also been demonstrated in the flexible transformation of the coupling products to meta-phenols and benzo[a]carbazoles.
Keyphrases
- electron transfer
- room temperature
- ms ms
- high performance liquid chromatography
- liquid chromatography tandem mass spectrometry
- signaling pathway
- molecular dynamics
- simultaneous determination
- gas chromatography mass spectrometry
- liquid chromatography
- tandem mass spectrometry
- mass spectrometry
- loop mediated isothermal amplification
- gas chromatography
- solid phase extraction
- life cycle