An Unprecedented Tandem Annulation of omega-Azido-1-alkynes with Diaryliodonium Salts: A Facile Synthesis of Polycyclic Quinolines

An Unprecedented Tandem Annulation of omega-Azido-1-alkynes with Diaryliodonium Salts: A Facile Synthesis of Polycyclic Quinolines
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omega-叠氮基-1-炔烃与二芳基碘鎓盐前所未有的串联环化:多环喹啉的简便合成

DOI:
10.1055/s-0034-1379248
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发表时间:
2014
期刊:
影响因子:
2
通讯作者:
Hongmei Qu
Hongmei Qu
中科院分区:
化学4区
文献类型:
--
作者:
Junjie Chen;Chao Chen;Jing Chen;Hongpeng Gao;Hongmei Qu

文献摘要

相似文献

多取代喹啉是通过ω-叠氮基-1-炔与作为C2-结构单元的二芳基碘鎓盐的级联成环反应合成的。该反应在Cu(I)催化剂的作用下进行,操作简便,反应条件温和,收率高。
Polysubstituted quinolines are synthesized through an unprecedented cascade annulation of ω-azido-1-alkynes with diaryliodonium salts, which serve as C2-building blocks. The reaction proceeds smoothly and is catalyzed by Cu(I) catalysts to give various quinolines in good isolated yields with simple operation under mild conditions.