M. Shiri and M. A. Zolfigol, “Surfactant-Type Catalysts in Organic Reactions,” Tetrahedron, Vol. 65, No. 3, 2009, pp. 587-598. doi:10.1016/j.tet.2008.09.085
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.