Event submissions
Published
This submission belongs to the session a. General Organic Synthesis of the event The 11th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Nov, 2007
Citation
Claudia Della Rosa, Pedro M.E. Mancini, Maria Kneeteman, Different Behaviouof of Disubtituted Aromatic Heterocycles in Polar Diels-Alder Reactions, in Proceedings of The 11th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2007, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-11-01301
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Different Behaviouof of Disubtituted Aromatic Heterocycles in Polar Diels-Alder Reactions
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Claudia Della Rosa 1
Pedro M.E. Mancini 1
Maria Kneeteman 1
1. Área Química Orgánica- Departamento de Química- Facultad de Ingeniería Química, Universidad Nacional del Litoral. Santiago del Estero 2829- 3000 Santa Fe, Argentina
Abstract
Dienophilic behaviour of disubstituted aromatic heterocycles towards normal electron demand Diels-Alder reactions is studied under thermal conditions. Formation of pyrrolyl-thiophenes are observed only in the reactions of nitrothiophenes with isoprene.
Keywords
heterocycles
Diels-Alder
dienophiles
Quantitative Regeneration of Carbonyl Compounds from Oximes and hydrazones by Gaseous Nitrogen Dioxide
Isoprene-mediated lithiation of chiral N-alkylimidazoles