Abstract
A new series of pyrrolo[3′,4′:3,4]pyrrolo[1,2-a]furoquinolines/ phenanthrolines and pyrrolo[1,2-a]phenanthrolines were efficiently built up from an 8-hydroxyquinoline derivative or phenanthroline via 1,3-dipolar cycloaddition reaction involving non-stabilized azomethine ylides, generated in situ from the parent furo[3,2-h]quinoliniums/phenanthroliums, in presence of a copper(II) chloride-phenanthroline catalytic system. The methodology combines general applicability with high yields. © 2014 Paira et al.
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Paira, R., Anwar, T., Banerjee, M., Bharitkar, Y. P., Mondal, S., Kundu, S., … Mondal, N. B. (2014). Copper-phenanthroline catalysts for regioselective synthesis of pyrrolo[3′,4′:3,4]pyrrolo[1,2-a]furoquinolines/phenanthrolines and of pyrrolo[1,2-a]phenanthrolines under mild conditions. Beilstein Journal of Organic Chemistry, 10, 692–700. https://doi.org/10.3762/bjoc.10.62
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