Chemoselective synthesis of thieno [3,2-c] [1,8]naphthyridin-4(5H-ones by tandem cyclization

被引：5
|
作者：
Majumdar, Krishna C. [1 ]
Rafique-ul-Islam [1 ]
机构：
[1] Univ Kalyani, Dept Chem, Kalyani 741235, W Bengal, India
来源：
HETEROATOM CHEMISTRY | 2007年 / 18卷 / 01期
关键词：
D O I：
10.1002/hc.20234
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
A number of the thieno[3,2-c][1,8]naphthyridin-4(5H)-ones are chemoselectively synthesized from 4-(4'-aryloxybut-2'-ynylthio)-l-phenyl-1,8-naphthyridin-2(1H)-ones in 82-90% yield by the formation of sulfoxide, followed by [2,3] and [3,3]sigmatropic rearrangement and an intramolecular Michael addition. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码：87 / 92
页数：6
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