Abstract
Condensation of cyclic ketones 1 with ethanolamines gave the corresponding spiro-oxazolidines 2. The thioamides 3 were obtained in good yields through reaction of 2 with the appropriate isothiocyanate. Reaction of 2 with formaldehyde or acetaldehyde in the presence of the appropriate amine afforded the corresponding aminomethyl spiro-compounds 4 and 5 respectively, in excellent yields. The structures of the isolated compounds were fully determined by spectral methods. Antimicrobial activities of some oxazolidines were also discussed.
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CITATION STYLE
Faidallah, H. M., Sharshira, E. M., & Al-Saadi, M. S. M. (2009). Synthesis and biological evaluafion of some new alicyclicspiro-2′- (1′, 3′ -oxazolidine) derivatives. Heterocyclic Communications, 15(1), 43–50. https://doi.org/10.1515/hc.2009.15.1.43
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