Regioselective 5-exo-Trig Heterocyclization of 2-Allyl-1-naphthols under the Influence of N-Iodosuccinimide or Molecular Iodine in Aqueous Micelle
Author(s) -
Pradipta K. Basu,
Amrita Ghosh
Publication year - 2012
Publication title -
organic chemistry international
Language(s) - English
Resource type - Journals
eISSN - 2090-2018
pISSN - 2090-200X
DOI - 10.1155/2012/810476
Subject(s) - regioselectivity , chemistry , iodine , naphthalene , pulmonary surfactant , aqueous solution , micelle , medicinal chemistry , organic chemistry , combinatorial chemistry , catalysis , biochemistry
Regioselective iodocyclization of a series of allylhydroxy naphthalene precursors involving N-iodosuccinimide and environment friendly green approach associated with surfactant-promoted molecular-iodine-mediated 5-exo-trig cyclization strategies has been explored
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