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M. S. Heller, “Synthesis of N-Alkyl- and N-Ary- lsulfonylphthalimides from Potassium Phthalimide and Sulfonyl Chlorides,” Journal of Chemical & Engineering Data, Vol. 15, No. 2, 1970, pp. 351-352. doi:10.1021/je60045a007

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.