期刊
CHEMICAL COMMUNICATIONS
卷 56, 期 9, 页码 1440-1443出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc08372c
关键词
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资金
- SERB, India [CRG/2018/000630]
- DST, India [SR/FST/CSII-026/2013]
- CSIR
- IIT Kharagpur
An efficient Rh(iii)-catalyzed straightforward strategy was developed for the tandem C4 arylamination/annulation of indole derivatives with anthranil to provide indoloquinoline moieties. This method is simple and regioselective with a wide scope and functional group tolerance. Mechanistic studies revealed the important role of the newly installed azacycle in the conversion of O-protected aldoximes to their cyano derivatives. Studies were carried out to explore the promising photophysical properties of the obtained indoloquinoline derivatives.
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