Benzocarbazole Synthesis via Visible-Light-Accelerated Rh(III)-Catalyzed C-H Annulation of Aromatic Amines with Bicyclic Alkenes.
Yichun WangDeyang JiaJing ZengYuming LiuXiubin BuXiaobo YangPublished in: Organic letters (2021)
A visible-light-accelerated Rh(III)-catalyzed C-H annulation of aromatic amines with bicyclic alkenes for the synthesis of benzocarbazole derivatives was developed. In this approach, with the cooperation of rhodium catalysis and visible-light irradiation, various aromatic amines reacted with oxabicyclic alkenes and azabicyclic alkenes smoothly at room temperature, delivering the corresponding bridged oxa or aza tetrahydro benzocarbazoles in good to excellent yields. Moreover, a series of benzo[b]carbazoles were synthesized conveniently through further aromatization in one pot. The potential of this method was demonstrated via directing-group removal, derivatization, a scale-up reaction, and fluorescence investigations.
Keyphrases
- visible light
- room temperature
- amino acid
- ionic liquid
- ms ms
- single molecule
- acinetobacter baumannii
- high performance liquid chromatography
- simultaneous determination
- mass spectrometry
- drug resistant
- multidrug resistant
- klebsiella pneumoniae
- radiation induced
- tandem mass spectrometry
- risk assessment
- gas chromatography mass spectrometry
- climate change
- pseudomonas aeruginosa
- energy transfer