Abstract
2-(2-furyl)phenanthro[9,10-d]oxazole was synthesized by the reaction of 9,10-phenanthrenequinoneimine and furan-2-carbaldehyde in ethanol. Reactions of electrophilic substitution of this compound were investigated (nitration, bromination, sulfurization, formylation, acylation). Depending on the reaction conditions the electrophile attacks either the furan ring or the phenanthrene fragment.
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Original Russian Text © A.A. Aleksandrov, M.M. Elchaninov, 2015, published in Zhurnal Organicheskoi Khimii, 2015, Vol. 51, No. 5, pp. 676–678.
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Aleksandrov, A.A., Elchaninov, M.M. Synthesis and reactivity of 2-(2-furyl)phenanthro[9,10-d]oxazole. Russ J Org Chem 51, 657–659 (2015). https://doi.org/10.1134/S1070428015050127
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DOI: https://doi.org/10.1134/S1070428015050127