Article citationsMore>>

K. C. Majumdar, U. K. Kundu, U. Das, N. K. Jana and B. Roy, “N-Iodosuccinimide—An Effective Reagent for Regioselective Heterocyclization of o-cyclohex-2-enylanilines for the Synthesis of hexahydrocarbazoles,” Canadian Journal of Chemistry, Vol. 83, No. 1, 2005, pp. 63-67. doi:10.1139/v04-162

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.