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1,6-Electrocyclization Reactions of Acceptor-substituted 2,3-Divinylindoles to Functionalized Carbazoles
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1990
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Heterocyclic1,6-Electrocyclization ReactionsThermal 1,6-Electrocyclization ReactionsOrganic ChemistryChemistryHeterocycle ChemistryPharmacologyDerivative (Chemistry)Carbazole AlkaloidsCarbazole Derivatives
The syntheses and thermal 1,6-electrocyclization reactions of acceptor-substituted 2.3-divinylindales, which give rise to functionalized carbazole derivatives, are described.Functionalized and/or annellated carbazoles and carbazole alkaloids have now attained considerable interest as pharmacologically active lead substances as well as being, for example, compounds with antibiotic and anti-tumour Hence.there is a still a major requirement for short and highly selective syntheses of these classes of heterocyclic compounds starting from readily available substrates.In continuation of our work on convergent pericyclic methods for the