The Synthesis and Characterization of Selected Optically Active Sulfoxides Bearing Perfluorocumyl Moiety, Their Spontaneous Reversible Transformations into Higher-Valent Organosulfur Species–Bicyclic Hydroxysulfuranes, and Their Irreversible Transfor

The preparation of the novel optically active sulfoxides (-)-(<i>S</i>)-1,1,1,3,3,3-hexafluoro-2-[<i>o</i>-(<i>p</i>-tolylsulfinyl)phenyl]propan-2-ol <b>1</b>, (-)-(<i>S</i>)-1,1,1,3,3,3-hexafluoro-2-[<i>o</i>-(methylsulfinyl)phenyl]propan-2-ol <b>2</b> and (-)-(<i>S</i>)-1,1,1,3,3,3-hexafluoro-2-[<i>o</i>-(<i>t</i>-butyl-sulfinyl)phenyl]propan-2-ol <b>3</b> according to the Andersen methodology and their spectroscopic characterization is presented. The NMR and CD spectroscopic evidence of the existence of the equilibrium between sulfoxide and hypervalent sulfurane forms of these compounds in solution and attempts at the isolation of corresponding sulfuranes are shown. For compound <b>3</b>, the unprecedented subsequent irreversible transformation in solution into corresponding cyclic sulfinate ester-sultine <b>17</b> was established on the basis of NMR spectroscopy measurements. The mechanism of this transformation was investigated by means of GC-MS analysis and confirmed on the basis of synthesized long alkyl chain analog <b>23</b> transformation in solution. Moreover, the oxidation properties of obtained sulfoxides <b>2</b> and <b>3</b> for the selected compounds are described.