Heck-type hydroarylations and 1,3-dipolar cycloaddition reactions of new tricyclic hydrazones

被引：8
|
作者：
Gul, Melek [1 ]
Ocal, Nuket [1 ]
机构：
[1] Yildiz Tech Univ, Fac Art & Sci, Dept Chem, TR-34210 Istanbul, Turkey
来源：
CANADIAN JOURNAL OF CHEMISTRY | 2010年 / 88卷 / 04期
关键词：
tricyclic hydrazone; reductive Heck reactions; C-C coupling; nitrile oxides; isoxazolines; IRON CHELATORS; CHEMISTRY; EPIBATIDINE;
D O I：
10.1139/V09-179
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
The C-C coupling of the new tricyclic hydrazones 3-7 with aryl and heteroaryl halides gave under reductive Heck conditions the tricyclic 1-(arylideneamino)pyrolidine-2,5-diones 8-11a, 9-11b, 10c, and 12. The [3+2] cycloadditions of 3-7 with p-chlorophenyl nitrile oxide (13) yielded the bridged isoxazoline derivatives 14-18 with potential biological activity.
引用
收藏
页码：323 / 330
页数：8
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