The Cope rearrangement is a classic pericyclic reaction that involves the intramolecular rearrangement of a 1,5-diene system. It's a sigmatropic rearrangement and can result in the formation of new carbon-carbon bonds and changes in the connectivity of atoms within the molecule.
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(4S,5R,E)-methyl 5-(cyclopent-1-en-1-yl)-5-methoxy-4-(4-methoxyphenyl)pent-2-enoate
Benzene, 1,1'-(1,4-diethylidene-1,4-butanediyl)bis[4-methoxy-, (Z,Z)-
2,5-diphenylhexa-1,5-diene-1,6-13C2
4,4-Dimethyl-5-oxo-2-phenethyl-tetrahydro-furan-3-carboxylic acid ethyl ester
