Conclusions
The differences in the34P NMR spectra of the isomeric triphosphites C13H27O9P3 which are formed by transesterification of triethyl phosphite with pentitols are caused by the different configurations of the ethyl phosphite rings.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 847–850, April, 1988.
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Makarova, N.A., Mukmenev, É.T. & Arbuzov, B.A. Structure of products from the transesterification of triethyl phosphite with pentitols. Russ Chem Bull 37, 727–730 (1988). https://doi.org/10.1007/BF01455487
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DOI: https://doi.org/10.1007/BF01455487