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K. B. Sharpless and M. W. Young, “Olefin Synthesis. Rate Enhancement of the Elimination of Alkyl Aryl Selenoxides by Electron-Withdrawing Substituents,” The Journal of Organic Chemistry, Vol. 40, No. 7, 1975, p. 947-949. doi:10.1021/jo00895a030

has been cited by the following article:

• TITLE: Synthesis, Spectral Characterization and Ligation of N-[2-(Phenylseleno)ethyl]phthalimide

  AUTHORS: Rupali Rastogi, Sanjay Kumar Srivastava, Shikha Asolia, Raymond J. Butcher

  KEYWORDS: Phthalimide; Selenium; Monoclinic; Phenylseleno; Sodium Borohydride

  JOURNAL NAME: Journal of Crystallization Process and Technology, Vol.3 No.1, January 28, 2013

  ABSTRACT: PhSe-Na+ generated in situ by reduction of PhSeSePh, with sodium borohydride on reaction with N-(2-bromoethyl) phthalimide in N2 atmosphere results in the formation of N-[2-(phenylseleno)ethyl]phthalimide (L1). The title compound has been characterized by elemental analysis, FT-IR, 1H and 13C NMR techniques. The crystal structure of L1 has been solved by direct methods and refined by full-matrix least squares. The ligand L1 crystallize in the monoclinic space group. Selenium forms two Se-C linkages, one is due to Se-Calkyl and the other one to Se-Caryl. Further, the ligation reaction of L1 with complex 1 is also explored whose identities are characterized by spectroscopic techniques.