磺酰
化学
组合化学
催化作用
反应条件
药物化学
立体化学
有机化学
烷基
作者
Shivam Pandey,Sabiha Parveen,Chandra M. R. Volla
标识
DOI:10.1002/asia.202300614
摘要
Herein, we developed an efficient approach to access biologically relevant 2-aminoquinolines and 1-aminoisoquinolines from readily available N-sulfonyl-1,2,3-triazoles and 2-quinolones or 1-isoquinolones. This transformation involves the selective O-H insertion of these derivatives onto the in situ generated Rh-azavinyl carbenes (Rh-AVC) followed by rearrangement. The reaction proceeds smoothly under operationally simple conditions and the protocol was found to be scalable.
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