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K. Oda, Y. Yamaguchi, T. Yoshimura, K. Wada and N. Nishizono, “Synthetic Models Related to Furanocoumarin-CYP 3A4 Interactions. Comparison of Furanocoumarin, Coumarin, and Benzofuran Dimers as Potent Inhibitors of CYP3A4 Activity,” Chemical and Pharmaceutical Bulletin, Vol. 55, No. 9, 2007, pp.1419-1421. doi:10.1248/cpb.55.1419

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.