EventsThe 13th International Electronic Conference on Synthetic Organic Chemistry
Event submissions
Published
with-doi10.3390/ecsoc-13-00165
This submission belongs to the session a. General Organic Synthesis of the event The 13th International Electronic Conference on Synthetic Organic Chemistry
Published date
31 Oct, 2009
Citation
Pedro Mancini, Maria Kneeteman, Claudia Della Rosa, 2-NITROBENZOFURAN AS DIENOPHILE IN DIELS-ALDER REACTIONS. A SIMPLE DIBENZOFURANS SYNTHESIS, in Proceedings of The 13th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2009, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-13-00165
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2-NITROBENZOFURAN AS DIENOPHILE IN DIELS-ALDER REACTIONS. A SIMPLE DIBENZOFURANS SYNTHESIS

Pedro Mancini 1
Maria Kneeteman 1
Claudia Della Rosa 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
2-nitrobenzofuran is studied in Diels-Alder reactions under thermal conditions. A concise synthesis of dibenzofurans has been developed via cycloaddition reactions.
Keywords
2-nitrobenzofuran
dienophiles
Diels-Alder
Efficient Catalytic Synthesis of primary Carbamates using Preyssler heteropolyacid catalyst, H14[NaP5W30O110] under solvent-free and in Green conditions
Asymmetric Synthesis of 1- ,3- or 4-Alkyl- or Aryl- Tetrahydro-Benzo[c]azepines