EventsThe 18th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session c. Microwave Assisted Synthesis of the event The 18th International Electronic Conference on Synthetic Organic Chemistry
Published date
05 Nov, 2014
Citation
Anna Francesca López Baena, Claudia Della Rosa, Maria Kneeteman, Pedro Mancini, Guillermo Gamboa, Microwave Irradiation: Polar Diels-Alder Reactions Using Nitropyrrole and Nitroindole Derivates as Electrophiles, in Proceedings of The 18th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2014, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-18-c014
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Microwave Irradiation: Polar Diels-Alder Reactions Using Nitropyrrole and Nitroindole Derivates as Electrophiles

Pedro Mancini 1
Maria Kneeteman 1
Claudia Della Rosa 2
Guillermo Gamboa 2
1. Universidad Nacional del Litoral-CONICET
2. Universidad Nacional del Litoral
Abstract
In this work we studied the influence of the microwave irradiation in polar Diels-Alder reactions between nitropyrrole and nitroindole derivatives acting as electrophiles with dienes of different nucleophilicity. The cycloadditions was performed under two conditions using benzene as the reaction medium and solvent free. The results clearly confirm that the use of microwave irradiation in this type of reactions have advantages in relation to the carried out under classical heating, though in general the products obtained are similar, but with lower reaction times and increases in the yield.
Keywords
Nitropyrrole
nitroindole
Diels-Alder
free-solvent
microwave
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