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H. J. Patel, J. Sarra, F. Caruso, M. Rossi, U. Doshi and R. A. Stephani, “Synthesis and Anticonvulsant Activity of New N-1’,N-3’-Disubstituted-2’H,3H,5’H-Spiro-(2-benzofuran-1,4’-imidazolidine)-2’,3,5’-triones,” Bioorganic & Medicinal Chemistry Letters, Vol. 16, No. 17, 2006, pp. 4644-4647. doi:10.1016/j.bmcl.2006.05.102

has been cited by the following article:

• TITLE: Iodocyclization of Diallyl-Dihydroxy Naphthalenes Using N-Iodosuccinimide vs Molecular Iodine in Aqueous Micelle

  AUTHORS: Pradipta Kumar Basu, Amrita Ghosh

  KEYWORDS: Di-Allyl-Dihydroxy Naphthalene; N-Iodosuccinimide; CTAB; Micelle; 5-Exo-Trig Mode; Regioselective Cyclization

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.3 No.3, August 27, 2013

  ABSTRACT: A number of doubly-fused [1,2] naphthodifurans have been synthesized from the corresponding diallyl-dihydroxy naphthalene precursors involving N-iodosuccinimide in acetonitrile and also by molecular iodine in aqueous micelle using CTAB as surfactant. The electrophilic cyclization occurs regioselectively by a 5-exo-trig mode of cyclization.