40167-15-5Relevant academic research and scientific papers
The synthesis of sulfinylphthalimides and their reactions with some nucleophiles in dioxane
Bozkurt, Yasemin Soydas,Kutuk, Halil
body text, p. 2250 - 2257 (2012/03/27)
In this study, some N-(p-substituted-arylsulfinyl)phthalimides (1a-1e) were synthesized. The synthesized compounds were examined with respect to their substitution reactions with sodium ethoxide, sodium methoxide, methylamine, and t-butylamine in dioxane.
Kinetics and mechanisms of the acid-catalyzed hydrolyses of N-(4-substituted-arylsulfinyl)phthalimides
Kutuk, Halil,Bekdemir, Yunus,Soydas, Yasemin
, p. 224 - 228 (2007/10/03)
The acid-catalyzed hydrolyses of N-(4-substituted-arylsulfinyl)phthalimides were studied in aqueous solutions of perchloric and sulfuric acids at 50.0 ± 0.1 and of hydrochloric acid at 40.0 ± 0.1°C. Analysis of the data by the Cox-Yates excess acidity method and substituent, temperature and solvent isotope effects indicate hydrolysis by an A2 mechanism at low acidity. At higher acidities a changeover to an A1 mechanism is observed. Copyright
Some Studies on Peptide Analogues Involving the Sulphinamide Group
Merricks, David,Sammes, Peter G.,Walker, Edward R. H.,Henrick, Kim,McPartlin, Mary M.
, p. 2169 - 2176 (2007/10/02)
The title compounds are of interest as possible transition state inhibitors of peptidases.A route to N-(alkylsulphinyl)amino acids is described.A method for generating α-benzamidosulphinamides is reported; a general route to such systems failed owing to t
