14933-92-7Relevant articles and documents
SULFENAMIDES AND SULFINAMIDES VIII. THE CHROMATOGRAPHY OF ARYL SULFENAMIDES
Chan, Christopher,Cole, Edward R.,Southwell-Keely, Peter T.
, p. 63 - 74 (2007/10/02)
Substituent effects with respect to position and extent of substitution in a series of N-aryl benzenesulfenamides (ArSNHAr') have been examined over several chromatographic systems.In normal phase TLC, although methyl substitution in either ring leads to
2-(4-Pyridyl)ethyl as a Protective Group for Sulfur Functionality
Katritzky, Alan R.,Takahashi, Ichiro,Marson, Charles M.
, p. 4914 - 4920 (2007/10/02)
2-(4-Pyridyl)ethyl sulfides have been prepared from a variety of alkyl and aryl thiols and from alkyl and acyl halides.These sulfides and their corresponding sulfoxides and sulfones were each depyridylethylated by quaternization and subsequent treatment with mild base to give respectively the thiols, sulfenic acids, sulfinic acids, and sulfenamides.During one of these protection-deprotection sequences, methyl 1-octyl sulfoxide was readily converted by aerial oxidation into the corresponding sulfone.
