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Y.-K. Lee, M.-H. Woo, C.-H. Kim, Y. Kim, S.-H. Lee, B.-S. Jeong, H.-W. Chang and J.-K. Son, “Two New Benzofurans from Gastrodia Elata and Their DNA Topoisomerases I and II Inhibitory Activities,” Planta Medica, Vol. 73, No. 12, 2007, pp. 1287-1291. doi:10.1055/s-2007-981619

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.