Diels Alder Reaction

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Details

The Diels-Alder reaction is an organic chemical reaction (specifically, a cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene system. The reaction can proceed even if some of the atoms in the newly-formed ring are not carbon. Some of the Diels-Alder reactions are reversible; the decomposition reaction of the cyclic system is then called the Retro-Diels-Alder. For example, Retro-Diels-Alder compounds are commonly observed when a Diels Alder product is analyzed via mass spectrometry. Otto Paul Hermann Diels and Kurt Alder first documented the novel reaction in 1928 for which they were awarded the Nobel Prize in Chemistry in 1950 for their work on the eponymous reaction.

Weitere Informationen

  • Allgemeine Informationen
    • GTIN 09786130728434
    • Editor Frederic P. Miller, Agnes F. Vandome, John McBrewster
    • Genre Chemie
    • Größe H7mm x B220mm x T150mm
    • EAN 9786130728434
    • Format Fachbuch
    • Titel Diels Alder Reaction
    • Gewicht 132g
    • Herausgeber Alphascript Publishing
    • Anzahl Seiten 84

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