Acenaphthenequinone reacted with diazofluorene, diphenyldiazomethane, phenybenzoyldiazomethane, phenacyl chloride, o-nitrobenzyl chloride, and diazohydroindenedione to give new oxadiazole, ketoepoxide and dioxadiazepine derivatives. They reacted with triphenylphosphine and triethylphosphite to give new organophosphorus compounds containing a six-membered or four-membered phosphorane ring. The structures were elucidated using IR, UV, NMR, and mass spectra, and elemental analyses.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1233–1243, August, 2009.
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El-Sawi, E.A., Mostafa, T.B. & Radwan, H.A. Phosphorylation of some new acenaphthenequinone derivatives. Chem Heterocycl Comp 45, 981–989 (2009). https://doi.org/10.1007/s10593-009-0363-y
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DOI: https://doi.org/10.1007/s10593-009-0363-y