Abstract
The rate of deuteration of 1-methyl-2-aryliminolactams depends on the electronic character of the substituent in the benzene ring and on the size of the lactam ring. Deuterium exchange proceeds at the highest rate in piperidine derivatives that have electron-donor substituents in the benzene ring.
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V. G. Granik, I. V. Persianova, and Yu. N. Sheinker, Khim. Geterotsikl. Soedin., 385 (1974).
Y. Tamura, Y. Yoshimura, and Y. Kita, Chem. Pharm. Bull.,19, 1068 (1971).
V. G. Granik, B. M. Pyatin, I. V. Persianova, E. M. Peresleni, N. P. Kostyuchenko, R. G. Glushkov (Gluschkov), and Y. N. Sheinker, Tetrahedron,26, 4367 (1970).
H. Meerwein, W. Florian, N. Schön, and G. Stopp, Ann.,641, 1 (1961).
A. I. Shatenshtein and E. N. Zvyagintseva, Dokl. Akad. Nauk SSSR,117, 852 (1957).
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See [1] for communication VIII.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 533–536, April, 1974.
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Granik, V.G., Zhidkova, A.M., Vlasova, T.F. et al. Lactam acetals. Chem Heterocycl Compd 10, 463–465 (1974). https://doi.org/10.1007/BF00945642
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DOI: https://doi.org/10.1007/BF00945642