%0 Journal Article
%T Iodocyclization of Diallyl-Dihydroxy Naphthalenes Using <i>N</i>-Iodosuccinimide vs Molecular Iodine in Aqueous Micelle
%A Pradipta Kumar Basu
%A Amrita Ghosh
%J International Journal of Organic Chemistry
%P 176-184
%@ 2161-4695
%D 2013
%I Scientific Research Publishing
%R 10.4236/ijoc.2013.33022
%X <span style=\"font-family:'Times New Roman','serif';color:black;font-size:10pt;\"><span style=\"font-family:Verdana;\">A number of doubly-fused [1,2] naphthodifurans have been synthesized from the corresponding diallyl-dihydroxy naphthalene precursors involving </span><i><span style=\"font-family:Verdana;\">N</span></i><span style=\"font-family:Verdana;\">-iodosuccinimide in acetonitrile and also by molecular iodine in aqueous micelle using CTAB as surfactant. The electrophilic cyclization occurs regioselectively by a 5-</span><i><span style=\"font-family:Verdana;\">exo</span></i><span style=\"font-family:Verdana;\">-trig mode of cyclization.</span></span>
%K Di-Allyl-Dihydroxy Naphthalene
%K &lt
%K i&gt
%K N&lt
%K /i&gt
%K -Iodosuccinimide
%K CTAB
%K Micelle
%K 5-&lt
%K i&gt
%K Exo&lt
%K /i&gt
%K -Trig Mode
%K Regioselective Cyclization
%U http://www.scirp.org/journal/PaperInformation.aspx?PaperID=36287