Domino ring-opening/recyclization reactions of doubly activated cyclopropanes as a strategy for the synthesis of furoquinoline derivatives

被引:113
作者
Zhang, Zhiguo [1 ]
Zhang, Qian [1 ]
Sun, Shaoguang [1 ]
Xiong, Tao [1 ]
Liu, Qun [1 ]
机构
[1] NE Normal Univ, Dept Chem, Changchun 130024, Peoples R China
关键词
cyclization; cyclopropanes; domino reactions; furoquinolines; synthetic methods;
D O I
10.1002/anie.200604276
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Chemical Equation Presented) In one easy step, doubly activated cyclopropanes 1 can be transformed into furoquinoline derivatives 2 through a tandem ring-opening/recyclization reaction mediated by SnCl4·5 H2O. A variety of substrates 1 derived from cheap starting materials were converted into the corresponding furoquinolines in good to excellent yields with high chemo- and regioselectivity. R = H, Me, OMe, Cl, or aromatic group is naphthyl. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:1726 / 1729
页数:4
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