Hf(OTf)4-Catalyzed 1,6-Conjugate Addition of 2-Alkyl-azaarenes to para-Quinone Methides.
Xinyuan LiuBinbin LiuZhan ShiChen TanRong FanZhi LiJiajing TanPublished in: The Journal of organic chemistry (2021)
Herein we reported a Hf(OTf)4-catalyzed carbon-carbon bond formation reaction between 2-alkyl-azaarenes and para-quinone methides (p-QMs). This 1,6-conjugate addition protocol offered rapid access to a large array of triarylethane products in good yields. The catalyst loading could be reduced to 1 mol %. Studies pertinent to scale-up reaction and product derivatization were also presented.
Keyphrases
- room temperature
- ionic liquid
- cancer therapy
- visible light
- ms ms
- acute heart failure
- randomized controlled trial
- electron transfer
- liquid chromatography tandem mass spectrometry
- high throughput
- high performance liquid chromatography
- high resolution
- gas chromatography mass spectrometry
- liquid chromatography
- highly efficient
- heart failure
- reduced graphene oxide
- loop mediated isothermal amplification
- tandem mass spectrometry
- carbon dioxide
- high density
- metal organic framework
- transition metal