56355-59-0Relevant academic research and scientific papers
The chemistry of 5-oxodihydroisoxazoles. Part 19. The synthesis and photolysis of N-thioacylisoxazol-5(2H)-ones
Prager, Rolf H.,Taylor, Max R.,Williams, Craig M.
, p. 2673 - 2678 (2007/10/03)
5-Oxodihydroisoxazoles react with thiocarbonyl chlorides to afford N-thioacylisoxazol-5(2H)-ones which lose carbon dioxide under photochemical conditions and undergo intramolecular cyclisation of the iminocarbene to afford thiazoles. However, in some cases loss of carbon dioxide is accompanied by loss of sulfur, giving 1,3-oxazin-6-ones. Copyright 1997 by the Royal Society of Chemistry.
Cyclopropyl derivative lipoxygenase inhibitors
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, (2008/06/13)
Certain carbocyclic aryl- and heterocyclic aryl- substituted cyclopropyl N-hydroxyureas, N-hydroxy-carboxamides, and N-acyl-N-hydroxyamines inhibit 5- and/or 12-lipoxygenase and are useful in the treatment of inflammatory disease states.
