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P. J. DeChristopher, J. P. Adamek, G. D. Lyon, S. A. Klein and R. J. Baumgarten, “Simple Deaminations. V. Preparation and Some Properties of N-Alkyl-N,N-Dis- ulfonimides,” Journal of Organic Chemistry, Vol. 39, No. 24, 1974, pp. 3525-3532. doi:10.1021/jo00938a017

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.