The Diels-Alder reaction is a well-known organic chemical reaction that involves the formation of a new six-membered ring from a conjugated diene (a molecule with two double bonds) and a dienophile (a molecule that readily reacts with a diene). An intramolecular Diels-Alder reaction means that both the diene and the dienophile are present within the same molecule, which leads to the formation of a ring within that molecule.
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3-(3-butynyloxy)-5-chloro-6-methyl-1-phenyl-2(1H)-pyrazinone
(E)-3-(1-Benzenesulfonyl-1H-indol-2-yl)-prop-2-en-1-ol
<α-(7-Oxo-1,3,5-cycloheptatrien-1-yloxy)benzyliden>propandinitril
1-(furan-2-yl)-N-(phenylmethyl)ethanamine
5-chloro-3-methoxy-6-methyl-1-phenyl-pyrazin-2(1H)-one
