56355-51-2Relevant articles and documents
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.
Heterocyclic alcohols and their derivatives
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, (2008/06/13)
Novel heterocyclic compounds of the formula STR1 wherein X is selected from the group consisting of chlorine, bromine, iodine and --OH, W is selected from the group consisting of hydrogen and --CN, Z is selected from the group consisting of --CH2/su