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- Q375669 subject Q6900265.
- Q375669 subject Q7458901.
- Q375669 subject Q8343673.
- Q375669 subject Q9006606.
- Q375669 abstract "The Diels–Alder reaction is an organic chemical reaction (specifically, a [4+2] cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene system. It was first described by Otto Diels and Kurt Alder in 1928, for which work they were awarded the Nobel Prize in Chemistry in 1950. The Diels–Alder reaction is particularly useful in synthetic organic chemistry as a reliable method for forming 6-membered systems with good control over regio- and stereochemical properties. The underlying concept has also been applied to other π-systems, such as carbonyls and imines, to furnish the corresponding heterocycles, known as the hetero-Diels–Alder reaction. Diels–Alder reactions can be reversible under certain conditions; the reverse reaction is known as the retro-Diels–Alder reaction.".
- Q375669 thumbnail Diels-alder_(1,3-butadiene_-_Ethylene).png?width=300.
- Q375669 wikiPageExternalLink endo_rule.pdf.
- Q375669 wikiPageExternalLink reaction.htm.
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- Q375669 type Thing.
- Q375669 comment "The Diels–Alder reaction is an organic chemical reaction (specifically, a [4+2] cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene system. It was first described by Otto Diels and Kurt Alder in 1928, for which work they were awarded the Nobel Prize in Chemistry in 1950.".
- Q375669 label "Diels–Alder reaction".
- Q375669 depiction Diels-alder_(1,3-butadiene_-_Ethylene).png.