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V. A. Mahajan, P. D. Shinde, A. S. Gajare, M. Karthikeyan and R. D. Wakharkar, “EPZ-10 Catalyzed Regioselective Transformation of Alkenes into β-Iodo Ethers, Iodohydrins and 2-Iodomethyl-2,3-dihydro Benzofurans,” Green Chemistry, Vol. 4, No. 4, 2002, pp. 325-327. doi:10.1039/b202725a

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.