'One-Pot' Synthesis of Sulphinic Esters from Disulphides
作者:Peter Brownbridge、Ian C. Jowett
DOI:10.1055/s-1988-27535
日期:——
Alkane- and arenesulphinic esters can conveniently be prepared from disulphides and alcohols using N-bromosuccinimide or a combination of 3-chloroperoxybenzoic acid and N-bromosuccinimide.
The reaction of singlet oxygen with tetrakis(ethylthio)ethylene has been shown to afford diethylthiooxalate and diethyl disulfide. The expected diethylthiocarbonate was also obtained as a minor product. A similar reaction with bis(ethylthio)ethylene gave ethylthioglyoxalate together with diethyl disulfide. Formation of diethylthioacetaldehyde was also observed, and is suggested to proceed via the intermediary
disulfides, sulfides and of n-butanethiol in alcohols or aqueous acetonitrile in the presence of oxygen was investigated : the corresponding sulfonic acids are produced in good yields for short alkyl chain compounds, together with smaller amounts of sulfuric and carboxylic acids. In acetonitrile, the influence of added water on the reaction course is evidenced : increased reaction rate and acid yields,
Wenschuh, Eberhard; Seidel, Wolfgang; Zschunke, Adolf, Phosphorus and Sulfur and the Related Elements, 1981, vol. 10, p. 21 - 26
作者:Wenschuh, Eberhard、Seidel, Wolfgang、Zschunke, Adolf、Kolbe, Alfred
DOI:——
日期:——
Stereoselective Synthesis of Racemic and Optically Active <i>E</i>-Vinyl and <i>E</i>-Dienyl Sulfoxides via Wittig Reaction of α-Sulfinyl Phosphonium Ylides
A series of ol-sulfinyl phosphonium ylides have been obtained in the reaction of phosphonium mono- and diylides with sulfinic acid esters. The use of(-)-(S)-menthyl-p-toluenesulfinate in this reaction afforded the corresponding (S)-((p-tolylsulfinyl)methyl)triphenylphosphonium ylide. The Wittig reaction of these ylides with saturated and unsaturated aldehydes resulted in the formation of racemic and optically active (+)-(R)-vinyl and dienyl sulfoxides with the E-geometry. The synthesis of (+)-(R)-((p-tolylsulfinyl)methyl)triphenyl iodide as a precursor of the optically active ylide has also been described.