IJOC  Vol.3 No.3 , September 2013
Iodocyclization of Diallyl-Dihydroxy Naphthalenes Using N-Iodosuccinimide vs Molecular Iodine in Aqueous Micelle
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.

Cite this paper
P. Basu and A. Ghosh, "Iodocyclization of Diallyl-Dihydroxy Naphthalenes Using N-Iodosuccinimide vs Molecular Iodine in Aqueous Micelle," International Journal of Organic Chemistry, Vol. 3 No. 3, 2013, pp. 176-184. doi: 10.4236/ijoc.2013.33022.
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