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P. Monjoint and M. F. Ruasse, “Nucleophilic Substituon at Sulfonyl Sulfur Atom: Aminolysis of 1-Tosyl-3-Me- thyl Imidazolium Chloride in Aqueous Medium,” Tetr- ahedron Letters, Vol. 25, No. 30, 1984, pp. 3183-3186. doi:10.1016/S0040-4039(01)91003-2

has been cited by the following article:

• TITLE: The Synthesis of Arylsulfonylphthalimides and Their Reactions with Several Amines in Acetonitrile

  AUTHORS: Seyhan Ozturk, Halil Kutuk

  KEYWORDS: Arylsulfonyl Phthalimides, Mechanism, Substituent Effect, Activation Entropy

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.1 No.4, December 27, 2011

  ABSTRACT: In this study, several N-(p-substituted-arylsulfonyl)phthalimides (1a-e) were synthesized. The synthesized compounds were then examined with respect to their substitution reactions with t-butylamine, diethylamine, cyclohexylamine, and trans-1,2-diaminocyclohexane in acetonitrile. In order to determine the mechanism, substituent effect, activation entropy, and nucleophile effect were used as criteria.