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G. F. Filzen, L. Bratton, X.-M. Cheng, N. Erasga, A. Geyer, C. Lee, G. Lu, J. Pulaski, R. J. Sorenson, P. C. Unangst, B. K. Trivedi and X. Xu, “Synthesis and SAR of Selective Benzothiophene, Benzofuran, and Indole-Based Peroxisome Proliferator-Activated Receptor δ Agonists,” Bioorganic & Medicinal Chemistry Letters, Vol. 17, No. 13, 2007, pp. 3630-635. doi:10.1016/j.bmcl.2007.04.047

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.