Conclusions
2-Qxo-3-methyl-5-chloro-3-hexene and trans-2-oxo-5-chloro-3-heptene, adequate low-molecular-weight models of labile carbonylallyl groups in poly(vinyl chloride) macromolecules, were synthesized. Tributyl phosphite reacts with the model compounds at the oxovinylene fragment via a step of formation of intermediate phosphorane structures, which are converted to stable ketophosphonates during heating.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1106–1108, May, 1985.
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Mukmeneva, N.A., Cherezova, E.N., Yamalieva, L.N. et al. Reaction of oxochloroalkenes with phosphorous acid esters. Russ Chem Bull 34, 1009–1011 (1985). https://doi.org/10.1007/BF01142792
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DOI: https://doi.org/10.1007/BF01142792