Article citationsMore>>

M. Ettaoussi, B. Peres, D. Klupsch, P. Delagrange, J.-A. Boutin, P. Renard, D.-H. Caignard, P. Chavatte, P. Berthelot, D. Lesieur and S. Yous, “ Design and Synthesis of Benzofuranic Derivatives as New Ligands at the Melatonin-Binding Site MT3,” Bioorganic & Medicinal Chemistry, Vol. 16, No. 9, 2008, pp. 4954-4962. doi:10.1016/j.bmc.2008.03.036

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.