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.
Keywords
Cycloaddition
Azomethine ylide
Nitrile
Tricyclic
Chemistry
Ylide
Ring (chemistry)
1,3-Dipolar cycloaddition
Organic chemistry
Catalysis
Subject Areas
Organic Chemistry Cycloaddition Reactions
·Organic Chemistry ·Physical Sciences
Synthesis and Reactions of Organic Compounds
·Organic Chemistry ·Physical Sciences
Synthesis and Catalytic Reactions
·Organic Chemistry ·Physical Sciences
Citations by Year
2015: 2
2017: 1
2024: 1
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