Abstract

The reaction of the intermediate ketene N,Se-hemiacetal 3, prepared from cyanomethylene derivatives 1 by treatment with Et3N and aryl isoselenocyanates 2, with bis-electrophiles 6, 7, 9, and 11 in DMF affords tetrahydro-1H-1,3-selenazine (= 1,3-selenazinane) derivatives 8, 10, and 12 in good yield (Scheme 2 and Tables 1 – 3). Chemical and spectroscopic evidence for the structures of the new compounds are described. The structures of 8d and 12e are established by X-ray crystallography (Figs. 1 and 2)

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