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(N‐Heterocyclic Carbene)Gold(I)‐Catalyzed Cycloisomerization of Cyclohexadienyl Alkynes to Tetracyclo[3.3.0.0<sup>2,8</sup>.0<sup>4,6</sup>]octanes
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Citations
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References
2007
Year
Chemical EngineeringNovel OrganocatalystsCyclohexadienyl AlkynesEngineeringHeterocyclicAlkene MetathesisOpen-cage CompoundsOrganic ChemistryOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistryOpen-chain DieneGold Catalyst
Biscyclopropanation: Dienynes containing a cyclohexadienyl unit can be converted into tetracyclo[3.3.0.02,8.04,6]octanes by treatment with an (N-heterocyclic carbene)gold catalyst. When the dienynes bear an open-chain diene instead of cyclohexadiene, open-cage compounds, with two sides missing from the cage, are obtained.
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