Reductive Heck Reactions and [3+2] Cycloadditions of Unsaturated N,N'-Bistricyclic Imides

被引：0

作者：

Gul, Melek ^{[2
]}

Kulu, Irem ^{[1
]}

Gunkara, Omer Tahir ^{[1
]}

Ocal, Nuket ^{[1
]}

机构：

[1] Yildiz Tech Univ, Fac Sci & Arts, TR-34220 Esenler, Turkey

[2] Univ Amasya, Fac Sci & Arts, TR-05100 Amasya, Turkey

来源：

ACTA CHIMICA SLOVENICA | 2013年 / 60卷 / 01期

关键词：

Alkenes; cycloadditions; heterocycles; hydroarylations; triyclic imides; SUBSTITUTED CYCLIC IMIDES; HYDROARYLATION; EPIBOXIDINE; ANALOGS; DICARBOXIMIDES; ANTICANCER;

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The C-C coupling of N,N'-bis(5-norbornene-2,3-dicarboximide) (3) and N,N'-bis(7-oxa-5-norbornene-2,3-dicarboximide) (6) with aryl and heteroaryl iodides gave under reductive Heck conditions the C-aryl(hetaryl), substituted N,N'bistricyclic imides 7a-f and 8a,b. The fused spiro-1,3-indandionolylpyrrolidine compounds, 9, 10 and 11 were also obtained from ninhydrine, sarcosine and 3 or 6 via [3+2] cycloaddition.

引用

页码：87 / 94

页数：8

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