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1,7-Electrocyclic Reactions of α,β,γ,δ-Unsaturated 1,3-Dipoles as a Synthetic Route to Seven-Membered Heterocycles
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1991
Year
Diazoalkenes 3δ-Unsaturated 1,3-DipolesEngineeringHeterocyclicDiversity Oriented SynthesisNatural SciencesDiversity-oriented SynthesisOther 1,3-Dipoles 7Seven-membered HeterocyclesOrganic Chemistry1,7-Electrocyclic ReactionsGeneral Synthetic ToolChemistryHeterocycle ChemistryPharmacologySynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Various seven-membered heterocyclic compounds (monocyclic and annulated) are accessible by means of a general synthetic tool, i. e. 1,7-electrocyclic ring closure of 1,3-dipoles that are α,β, and γ,δ-unsaturated. 1. Introduction 2. Diazoalkenes 3. Nitrile Imines 4. Nitrile Ylides 5. Carbonyl Ylides 6. Other 1,3-Dipoles 7. Concluding Remarks