Diels–Alder reaction
In organic chemistry, the Diels–Alder reaction is a chemical reaction between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene derivative. It is the prototypical example of a pericyclic reaction with a concerted mechanism. More specifically, it is classified as a thermally-allowed [4+2] cycloaddition with Woodward–Hoffmann symbol [π4s + π2s]. It was first described by Otto Diels and Kurt Alder in 1928. For the discovery of this reaction, they were awarded the Nobel Prize in Chemistry in 1950. Through the simultaneous construction of two new carbon–carbon bonds, the Diels–Alder reaction provides a reliable way to form six-membered rings with good control over the regio- and stereochemical outcomes. Consequently, it has served as
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Alder-Stein rulesAlder–Stein rulesAsymmetric Diels-Alder reactionDiels-Adler reactionDiels-AlderDiels-Alder ReactionDiels-Alder additionDiels-Alder cyclizationDiels-Alder cycloaddition reactionDiels-Alder reactionDiels-Alder reactionsDiels AlderDiels Alder reactionDiels alders reactionDiels–AlderDiene synthesisDienophileEndo RuleEndo ruleRetro Diels AlderRetro Diels–Alder reactionRickert-Alder reactionSynthesen in der hydroaromatischen Reihe
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(4+3) cycloaddition1,2,3,4-Tetraphenylnaphthalene1,2,4,5-Tetrabromobenzene1,2-Cyclohexane dicarboxylic acid diisononyl ester1,3-Diphenylisobenzofuran1,3-Dipolar cycloaddition1,4-Benzoquinone1,4-Dioxin1,4-Naphthoquinone1,7-Octadiene1928 in science2,5-Dimethylfuran2-Pyrone3-Bromofuran4,7-Dihydroisoindole4-Phenyl-1,2,4-triazole-3,5-dione4-VinylcyclohexeneAbsinthinAcetylenedicarboxylic acidAcroleinAcrylonitrileAlder-Stein rulesAlder (surname)Alder–Stein rulesAldrinAlkeneAlkyneAlpha-beta Unsaturated carbonyl compoundsAnthraceneAnthraquinoneAromatic compoundArsabenzeneArtificial metalloenzymeAryneAscaridoleAsymmetric Diels-Alder reactionAtom economyAza-Diels–Alder reactionAzomethine ylideBTBP
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Diels–Alder reaction
In organic chemistry, the Diels–Alder reaction is a chemical reaction between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene derivative. It is the prototypical example of a pericyclic reaction with a concerted mechanism. More specifically, it is classified as a thermally-allowed [4+2] cycloaddition with Woodward–Hoffmann symbol [π4s + π2s]. It was first described by Otto Diels and Kurt Alder in 1928. For the discovery of this reaction, they were awarded the Nobel Prize in Chemistry in 1950. Through the simultaneous construction of two new carbon–carbon bonds, the Diels–Alder reaction provides a reliable way to form six-membered rings with good control over the regio- and stereochemical outcomes. Consequently, it has served as
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A reação de Diels-Alder, també ...... anto, envolvem maior energia .
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De diels-alderreactie is een o ...... de ontdekking van de reactie.
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Die Diels-Alder-Reaktion ist e ...... ist durchgängig hervorragend.
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Diels-Alder erreakzioa kimika ...... zken produktuan mantentzen da.
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Dielsova–Alderova reakce je re ...... s určitou zvláštní strukturou.
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Diels–Alderreaktionen är en or ...... till genom att lägga till den.
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In organic chemistry, the Diel ...... he retro-Diels–Alder reaction.
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La reacció de Diels-Alder és u ...... i Nobel de Química l'any 1950.
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La reacción Diels-Alder es una ...... nos de alcance o versatilidad.
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La reazione di Diels-Alder è u ...... ne definita Retro Diels-Alder.
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Cycloaddition
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A reação de Diels-Alder, també ...... oplamento de furano/maleimida.
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De diels-alderreactie is een o ...... e andere organische synthesen.
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Die Diels-Alder-Reaktion ist e ...... belpreis ausgezeichnet wurden.
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Diels-Alder erreakzioa kimika ...... alde erreakzioa errazten dute.
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Dielsova–Alderova reakce je re ...... eterocyklické sloučeniny. Reak
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Diels–Alderreaktionen är en or ...... till genom att lägga till den.
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In organic chemistry, the Diel ...... onsequently, it has served as
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La reacció de Diels-Alder és u ...... posició de l'anell s'anomena .
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La reacción Diels-Alder es una ...... do sustituido del ciclohexeno.
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La reazione di Diels-Alder è u ...... i formano anelli eterociclici.
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Diels-Alder erreakzio
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Diels-Alder-Reaktion
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Diels-alderreactie
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Dielsova–Alderova reakce
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Diels–Alder reaction
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Diels–Alderreaktion
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Reacció de Diels-Alder
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Reacción de Diels-Alder
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Reakcja Dielsa-Aldera
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Reaksi Diels-Alder
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