In this master thesis the investigation of transformation of α-oxoketene dithioacetals in the presence of iodine with pentafluorophenyl hydrazine is presented. It resulted in formation of 5-(methylsulfanyl)-1-(pentafluorophenyl)-1H-pyrazoles. Synthesis of α-oxoketene dithioacetals is also reported and discussed. Their transformation occured in aprotic solvents and with 40–60 mol% of iodine as promotor. Most reactions gave good yields. There is no clear correlation between the yield and stereoelectronic effects of the substituents. All new substances were characterised by 1H-, 13C- and 19F-NMR, IR spectroscopy, elemental analysis and/or mass spectrometry and by measuring their melting point.
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