- cycloheptadiene
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Any of several isomeric unsaturated alicyclic hydrocarbons having seven carbon atoms and two double bonds; any derivative of such compound
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cycloheptadiene
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Divinylcyclopropane-cycloheptadiene rearrangement — The divinylcyclopropane cycloheptadiene rearrangement is an organic chemical transformation that involves the isomerization of a 1,2 divinylcyclopropane into a cycloheptadiene or triene. It is conceptually related to the Cope rearrangement, but… … Wikipedia
Ectocarpene — Chembox new ImageFile1 = Ectocarpene.png ImageSize1 = ImageFile2 = Ectocarpene small.png ImageSize2 = IUPACName = (5S) 5 [(1E) but 1 en 1 yl] cyclohepta 1,3 diene OtherNames = (6R) 6 [(E) but 1 enyl] cyclohepta 1,4 diene, 6 [Z butenyl] 1,4… … Wikipedia
Cyclopentadiene — Cyclopentadiene … Wikipedia
Cyclopropane — Cyclopropane[1] … Wikipedia
Cyclopropene — Cyclopropene … Wikipedia
Cycloalkene — A cycloalkene or cycloolefin is a type of alkene hydrocarbon which contains a closed ring of carbon atoms, but has no aromatic character. Some cycloalkenes, such as cyclobutene and cyclopentene, can be used as monomers to produce polymer chains.… … Wikipedia
Cyclobutadiene — IUPAC name … Wikipedia
Cyclohexene — Cyclohexene … Wikipedia
Cyclobenzaprine — Systematic (IUPAC) name 3 (5H dibenzo[a,d]cyclohe … Wikipedia
Cope rearrangement — The Cope rearrangement is an extensively studied organic reaction involving the [3,3] sigmatropic rearrangement of 1,5 dienes.[1][2][3][4] It was developed by Arthur C. Cope. For example 3 methyl 1,5 hexadiene heated to 300°C yields 1,5… … Wikipedia
