H. Kutuk and S. Ozturk, “A Kinetic Study of Acid- Catalyzed Hydrolysis of Some Arylsulfonyl Phtha- limides,” Phosphorus, Sulfur, and Silicon and the Related Elements, Vol. 184, No. 2, 2009, pp. 332-340. doi:10.1080/10426500802119655

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.