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D. M. Schultz, J. A. Prescher, S. Kidd, D. Marona-Lewicka, D. E. Nichols and A. Monte, “‘Hybrid’ benzofuran-benzopyran congeners as rigid analogs of hallucinogenic phenethylamines,” Bioorganic & Medicinal Chemistry Letters, Vol. 16, No. 11, 2008, pp. 6242-6251. doi:10.1016/j.bmc.2008.04.030

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.