Abstract
1,2-O-Isopropylidene-α-D-glucofuranose 3,5,6-phosphite was stidied in reactions with α-dicarbonyl compounds. Reagents with the electron-acceptor halogen atom form with the former stable phosphoranes, while unsubstituted α-dicarbonyl compounds, the corresponding normal phosphates.
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REFERENCES
Koroteev, M.P. and Nifant'ev, E.E., Zh. Obshch. Khim., 1993, vol. 63, no. 3, pp. 481-521.
Nifantyev, E.E. and Koroteev, M.P., Rev. Sov. Sci., Sect. B, 1984, no. 5, pp. 399-442.
Kochetkov, N.K., Nifantyev, E.E., Koroteev, M.P., Zhane, Z.K., and Borisenko, A.A., Carbohydr. Res., 1976, vol. 47, pp. 221-231.
Nifant'ev, E.E., Koroteev, M.P., Pugashova, N.M., Bekker, A.R., Bel'skii, V.K., Magomedova, N.S., and Il'inets, A.M., Zh. Obshch. Khim., 1990, vol. 60, no. 6, pp. 1412-1419.
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Sychev, V.A., Koroteev, M.P., Dzgoeva, Z.M. et al. First Representatives of Stable Phosphoranes Derived from Bicyclophosphorylated Carbohydrates. Russian Journal of General Chemistry 71, 188–190 (2001). https://doi.org/10.1023/A:1012330901237
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DOI: https://doi.org/10.1023/A:1012330901237