Yu. V. Bakhtiyarova, M. S. Bondar, V. V. Andriyashin, O. N. Kataeva, I. V. Galkina, V. I. Galkin, “New phosphorus ylides in reactions of tertiary phosphines with phosphorylated quinone methide”, Mendeleev Commun., 19:1 (2009), 37

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D. W. Allen, Organophosphorus Chemistry, 2011, 1
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