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Microwave Irradiation: Polar Diels-Alder Reactions Using Nitropyrrole and Nitroindole Derivates as Electrophiles
Published:
05 November 2014
by MDPI
in The 18th International Electronic Conference on Synthetic Organic Chemistry
session Microwave Assisted Synthesis
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