An efficient domino one-pot synthesis of novel spirofuran-indenoquinoxalines by vinyltriphenylphosphonium salts

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Abstract

Abstract: A simple and convenient multi-component domino reaction has been described for the synthesis of novel spirofuran-indenoquinoxaline derivatives. Products were obtained by a three-component condensation reaction between ninhydrin, aromatic 1,2-diamines and dialkyl ethynedicarboxylates in the presence of a catalytic amount of triphenylphosphine in CH 2Cl 2 at ambient temperature in excellent yields. This one-pot process produces biologically and pharmacologically significant heterocycles with the formation of five new bonds (one C–C, two C=N and two C–O) and two new rings in a single operation. Graphical Abstract: [Figure not available: see fulltext.].

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Yazdani-Elah-Abadi, A., Maghsoodlou, M. T., Mohebat, R., & Heydari, R. (2017). An efficient domino one-pot synthesis of novel spirofuran-indenoquinoxalines by vinyltriphenylphosphonium salts. Journal of Chemical Sciences, 129(6), 691–698. https://doi.org/10.1007/s12039-017-1292-4

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