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Synthesis of tetrahydro-1,3,5-selenodiazine-2-selenones

G. Suchá r and R. Štefko

Department of Organic Chemistry and Biochemistry, Faculty of Natural Sciences, P. J. Šafárik University, 041 67 Košice

 

Abstract:  Phenyl isoselenocyanates in nucleophilic addition of sodium hydrogen selenide in the presence of salt of primary amine and formaldehyde react under the formation of 3,5-disubstituted tetrahydro-l13,5-selenodiazine-2-selenones. The structures of the synthesized compounds were proved by i.r., u.V., and 1H-n.m.r. spectra.

Full paper in Portable Document Format: 363a419.pdf

 

Chemical Papers 36 (3) 419–422 (1982)

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