化学
电泳剂
炔烃
薗头偶联反应
亲核细胞
三键
组合化学
卤素
碘化物
药物化学
有机化学
双键
烷基
催化作用
钯
作者
Guilherme Lutz,Fabíola Caldeira dos Santos,Davi F. Back,Mark S.B. Felix,Victor M. Deflon,Cristina W. Nogueira,Gilson Zeni
标识
DOI:10.1002/adsc.202401514
摘要
Abstract A methodology for the synthesis and functionalization of quinolines was developed. This approach involves the cyclization of 2‐amino arylalkynyl ketones to 3‐(organoselanyl)‐4‐iodoquinolines through a sequential reaction pathway. The process includes: (i) in situ formation of an electrophilic organoselenyl species, (ii) activation of the alkyne‘s carbon‐carbon bond via a seleniranium ion intermediate, (iii) anti‐nucleophilic attack of iodide on the activated triple bond, and (iv) subsequent condensation. The resulting 3‐(organoselanyl)‐4‐iodoquinolines were demonstrated to be versatile substrates, efficiently undergoing Sonogashira cross‐coupling to produce 4‐alkynyl‐quinolines and Ullmann‐type reactions to yield the corresponding sulfides. Furthermore, the 4‐alkynyl‐quinolines were readily converted into selenophene derivatives via halogen‐promoted electrophilic cyclization, highlighting the broad applicability of the developed method.
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