Collect. Czech. Chem. Commun.
2000, 65, 1630-1642
https://doi.org/10.1135/cccc20001630
Electrochemical Reductions of Methyl Azinyl Ketoximes on Mercury
Radek Cibulkaa, František Liškaa and Jiří Ludvíkb,*
a Department of Organic Chemistry, Institute of Chemical Technology, Prague, Technická 5, 166 28 Prague 6, Czech Republic
b J. Heyrovský Institute of Physical Chemistry, Academy of Sciences of the Czech Republic, Dolejškova 3, 182 23 Prague 8
References
1a. Feiters M. C. in: Comprehensive Supramolecular Chemistry (D. N. Reinhoudt, Ed.), Vol. 10, p. 321. Elsevier Science, Ltd., Oxford 1996 and references cited therein.
1b. Ridder A. M., Kellogg R. M. in: Comprehensive Supramolecular Chemistry (Y. Murakami, Ed.), Vol. 4, p. 402. Elsevier Science, Ltd., Oxford 1996 and references cited therein.
1c. Suh J.: Acc. Chem. Res. 1992, 25, 273 and references cited therein.
1d. Fendler J. H., Fendler E. J.: Catalysis in Micellar and Macromolecular Systems. Academic Press, New York 1975.
1e. Fendler J. H.: Membrane Mimetic Chemistry. Wiley, New York 1982.
2a. Langmuir 1999, 15, 405.
< F., Liška F., Mancin F., Tecilla P., Tonellato U.: https://doi.org/10.1021/la980861+>
2b. Collect. Czech. Chem. Commun. 1999, 64, 1159.
< R., Hampl F., Martinů T., Mazáč J., Totevová S., Liška F.: https://doi.org/10.1135/cccc19991159>
2c. J. Mol. Catal. 1996, 104, 201.
< J., Hampl F., Liška F., Scrimin P., Tecilla P., Tonellato U.: https://doi.org/10.1016/1381-1169(95)00258-8>
2d. Collect. Czech. Chem. Commun. 1997, 62, 1342.
< R., Dvořák D., Hampl F., Liška F.: https://doi.org/10.1135/cccc19971342>
3a. Acta Chem. Scand. 1959, 13, 249.
< H.: https://doi.org/10.3891/acta.chem.scand.13-0249>
3b. Tetrahedron Lett. 1968, 33, 3651.
< H.: https://doi.org/10.1016/S0040-4039(00)89771-3>
4a. J. Chem. Soc. 1956, 4180.
< H. J., Georgans W. P.: https://doi.org/10.1039/jr9560004180>
4b. Leibzon V. N.: Russ. J. Electrochem. (Transl. of Elektrokhimiya) 1996, 32, 11; and references cited therein.
5a. J. Indian Chem. Soc. 1995, 72, 615.
M. S. S., Reddy S. J.:
5b. Talanta 1968, 15, 1413.
< L. W., Cheney G. E.: https://doi.org/10.1016/0039-9140(68)80201-2>
5c. Electrochim. Acta 1983, 28, 325.
< M. A., Luque de Castro M. D., Valcarcel M.: https://doi.org/10.1016/0013-4686(83)85129-9>
6a. C. R. Acad. Sci., Ser. II 1956, 242, 1799.
J., Fournari P., Chané J. P.:
6b. Collect. Czech. Chem. Commun. 1960, 25, 871.
< J., Kubíček R., Šantavý F.: https://doi.org/10.1135/cccc19600871>
6c. Anal. Chim. Acta 1961, 25, 281.
< N. G., Cohen E. M.: https://doi.org/10.1016/0003-2670(61)80159-1>
7. C. R. Acad. Sci., Ser. II 1958, 246, 274.
J., Laviron E.:
8a. Collect. Czech. Chem. Commun. 1973, 38, 1358.
< O., Bělovský O., Rejmanová P: https://doi.org/10.1135/cccc19731358>
8b. J. Chem. Soc., Perkin Trans. 1 1998, 775.
< J., Martelli G., Savoia D.: https://doi.org/10.1039/a706244c>
9. J. Coord. Chem. 1990, 22, 183.
< M., Saarinen H., Korvenranta J.: https://doi.org/10.1080/00958979009408214>
10. Zuman P.: Substituent Effects in Organic Polarography, p. 169. Plenum Press, New York 1967.
11. CS MOPAC. CambridgeSoft Corporation, Cambridge 1996.
12a. J. Electroanal. Chem. 1998, 457, 177.
< J., Riedl F., Liška F., Zuman P.: https://doi.org/10.1016/S0022-0728(98)00305-2>
12b. Electroanalysis 1998, 10, 869.
< J., Riedl F., Liška F., Zuman P.: https://doi.org/10.1002/(SICI)1521-4109(199810)10:13<869::AID-ELAN869>3.0.CO;2-Y>
13. J. Magn. Reson., Ser. B 1993, 102, 241.
< V., Piotto R., Leppik S., Saudek V.: https://doi.org/10.1006/jmra.1993.1098>
14. Electrochim. Acta 1996, 41, 1661.
< J., Nygaard B.: https://doi.org/10.1016/0013-4686(95)00420-3>
15. Zuman P. in: Organic Electrochemistry (M. M. Baizer, Ed.), p. 155. Dekker, New York 1973.