Diels-Alder reaction

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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.

Diels-alder (1,3-butadiene - Ethylene).png

Quotes[edit]

  • When a mixture of 1,3-butadiene and ethene is heated in the gas phase, a remarkable reaction takes place in which cyclohexene is formed by the simultaneous generation of two new carbon – carbon bonds. This is the simplest example of the Diels-Alder reaction, in which a conjugated diene adds to an alkene to yield cyclohexene derivatives. The Diels-Alder reaction is in turn a special case of the more general class of cycloaddition reactions between psystems, the products of which are called cycloadducts.
    • K. Peter C. Vollhardt, Neil E. Schore (2011) Organic chemistry : structure and function 6th ed. Ch. 14 : Delocalized Pi Systems.

External links[edit]

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