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K. C. Majumdar and S. Sarkaroc, “N-Iodosuccinimide Mediated Regioselective Heterocyclization of 3-Cyclohex-2’-enyl-4-hydroxycoumarin,” Tetrahedron, Vol. 58, No. 42, 2002, pp. 8501-8504. doi:10.1016/S0040-4020(02)01024-4

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.