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3-carboxylate by using vicarious substitution of hydrogen, followed by intramolecular reductive heterocyclization. Some chemical properties of the target compound were characterized. As observed for the first time in the series… Click to show full abstract
3-carboxylate by using vicarious substitution of hydrogen, followed by intramolecular reductive heterocyclization. Some chemical properties of the target compound were characterized. As observed for the first time in the series of linear hetaryl-fused anthraquinones, the alkylation of hydroxy groups in naphtho[2,3-f]indole-5,10-diones gave not only 4,11-dialkoxy derivatives, but also the isomeric 5,10-dialkoxy derivatives of naphtho[2,3-f]indole-4,11-dione.
Keywords:
naphtho indole;
naphthacenequinone synthesis;
heterocyclic analogs;
indole carboxylic;
synthesis naphtho;
analogs naphthacenequinone
Journal Title: Chemistry of Heterocyclic Compounds
Year Published: 2017
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Journal Title: Chemistry of Heterocyclic Compounds
Year Published: 2017
Link to full text (if available)
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recommendations!