Abstract
Our research group has published numerous papers over the last three years on the reaction of nitrile oxides and azomethine ylide with unsaturated tricyclic N-substituted dicarboximides selected according to the importance of possible biological activities. These reactions cover full range of mechanistic pathways and timings of bond-forming processes to give five-membered ring closure by 1,3-dipolar cycloaddition.
Keywords: Azomethine ylide, biological active molecules, 1, 3-dipolar cycloaddition, hydrazones, isoxazolines, nitrile oxides, tricyclic imides.
Mini-Reviews in Organic Chemistry
Title:Cycloaddition Reactions of Some Tricyclic Imides
Volume: 10 Issue: 4
Author(s): Irem Kulu, Melek Gul, Omer Tahir Gunkara and Nuket Ocal
Affiliation:
Keywords: Azomethine ylide, biological active molecules, 1, 3-dipolar cycloaddition, hydrazones, isoxazolines, nitrile oxides, tricyclic imides.
Abstract: Our research group has published numerous papers over the last three years on the reaction of nitrile oxides and azomethine ylide with unsaturated tricyclic N-substituted dicarboximides selected according to the importance of possible biological activities. These reactions cover full range of mechanistic pathways and timings of bond-forming processes to give five-membered ring closure by 1,3-dipolar cycloaddition.
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Cite this article as:
Kulu Irem, Gul Melek, Gunkara Tahir Omer and Ocal Nuket, Cycloaddition Reactions of Some Tricyclic Imides, Mini-Reviews in Organic Chemistry 2013; 10 (4) . https://dx.doi.org/10.2174/1570193X113106660017
DOI https://dx.doi.org/10.2174/1570193X113106660017 |
Print ISSN 1570-193X |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6298 |
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