56355-51-2Relevant 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.
Novel cyclopropane carboxylic acid derivatives
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, (2008/06/13)
Novel isomers and mixtures thereof of cyclopropane carboxylic acid derivatives with a 3-unsaturated side chain of Z geometry of the formula STR1 wherein A' is STR2 wherein R13 is selected from the group consisting of hydrogen and CN and R is an optionally unsaturated alkyl of 1 to 18 carbon atoms having insecticidal and nematocidal activity as well as plant and animal acaricidal activity and their preparation.
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
Thiazole derivatives of benzoic and phenylalkanoic acids
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, (2008/06/13)
Thiazole derivatives represented by the general formula: STR1 wherein A is oxygen, sulfur, imino, or NR3, wherein R3 is C1-5 alkyl, C2-5 alkenyl, C3-5 alkynyl, C3
