Electrocyclic reactions
11 real reactions from the literature: 4π electrocyclization on cyclic conjugated dienes and cyclobutenes; 6π electrocyclization on conjugated trienes. Each scheme shows starting materials, conditions and products, with the yield and reference where the source reports them.
Printable worksheet (PDF): with or without products.
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4π electrocyclization: cyclopentadiene (a cyclic conjugated diene) with hν; THF gives bicyclo(2.1.0)pent-2-ene (the cyclobutene).
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6π electrocyclization: oxepin (a conjugated triene) with 6e dis gives benzene oxide (the cyclohexadiene). 91% yield.
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4π electrocyclization: (1Z,3E)-cycloocta-1,3-diene (a cyclic conjugated diene) with 80 C; 4e con gives the cyclobutene. 100% yield.
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6π electrocyclization: a conjugated triene with 60 C; 6e dis gives 5-tert-butyl-6-cyclohexylidenecyclohexa-1,3-diene (the cyclohexadiene). 91% yield.
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4π electrocyclization: a cyclobutene with mesitylene (solvent); 4e con gives the cyclic conjugated diene. 78% yield.
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6π electrocyclization: a conjugated triene with 60 C, PhMe gives the cyclohexadiene. 98% yield.
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4π electrocyclization: a cyclic conjugated diene with 100 C; 4e con gives the electrocyclic product.
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6π electrocyclization: a conjugated triene with 150 C; 6e dis gives 5,5-dimethyl-5H-benzocycloheptene (the cyclohexadiene).
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4π electrocyclization: a cyclic conjugated diene with hv; 4e dis gives the cyclobutene.
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6π electrocyclization: a conjugated triene with 225 C; 6e dis gives 1-ethyl-1,2-dihydronaphthalene (the cyclohexadiene).
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6π electrocyclization: 1,2-bis[(E)-prop-1-enyl]benzene (a conjugated triene) with 225 C; 6e dis gives the cyclohexadiene.