Metal-Free Iodine(III)-Promoted Synthesis of Isoquinolones

被引:49
作者
Chen, Zhi-Wei
Zhu, Yi-Zhou [1 ]
Ou, Jin-Wang
Wang, Ya-Ping
Zheng, Jian-Yu
机构
[1] Nankai Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, State Key Lab, Tianjin 300071, Peoples R China
关键词
N BOND FORMATION; C-H ACTIVATION; INTRAMOLECULAR OXIDATIVE CYCLIZATION; TOPOISOMERASE-I INHIBITORS; MEDIATED ALKYNE AMIDATION; ACID-DERIVATIVES; DIRECTING GROUP; O BOND; ANNULATION; FUNCTIONALIZATION;
D O I
10.1021/jo5020307
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A metal-free oxidative cycloaddition reaction of substituted benzamides and alkynes has been developed for the synthesis of isoquinolones by using bis(trifluoracetoxy)iodobenzene (PIFA) and trifluoroacetic acid (TFA). Under mild conditions, a wide variety of isoquinolones were conveniently prepared via oxidative annulation of simple N-methoxybenzamide and diarylacetylene or aryl/alkyl acetylene derivatives in yields up to 87%.
引用
收藏
页码:10988 / 10998
页数:11
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