Conclusions
-
1.
α-Ketophosphonic acids are synthesized by hydrogenation of their benzyl esters.
-
2.
The possibility of nonenzymatic transamination of α-ketophosphonic acids without rupure of the C-P bond is shown.
Similar content being viewed by others
Literature cited
M. I. Kabachnik and P. A. Rossiiskaya, Izv. Akad. Nauk SSSR, Ser. Khim., 364 (1945).
K. D. Berlin and H. A. Taylor, J. Am. Chem. Soc.86, 3862 (1964).
V. F. Cooke, W. Gerrard, and W. J. Green, Chem. Ind., 351 (1953).
N. N. Gulyaev, E. V. Sharkova, M. M. Dedyukina, E. S. Severin, and R. M. Khomutov, Biokhimiya,36, 1267 (1971).
E. J. Glamkowski, G. Gal, R. Purick, A. J. Davidson, and M. Sletzinger, J. Org. Chem.,35, 3510 (1970).
R. W. Balsiger, D. G. Jones, and J. A. Montgomery, J. Org. Chem.,24, 434 (1959).
K. D. Berlin, D. M. Helewege, and M. Nagabhushanam, J. Org. Chem.,30, 1265 (1965).
Yoshihiko Matsuo, J. Am. Chem. Soc.,79, 2016 (1957).
Author information
Authors and Affiliations
Additional information
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp.1391–1394, June, 1978.
The authors wish to thank A. T. Prudchenko for interpretation of the PMR spectra and I. A. Gandurina for plotting the TR spectra.
Rights and permissions
About this article
Cite this article
Khomutov, R.M., Osipova, T.I. & Zhukov, Y.N. Synthesis of α-ketophosphonic acids. Russ Chem Bull 27, 1210–1213 (1978). https://doi.org/10.1007/BF00923378
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00923378