Article citationsMore>>

K. C. Majumdar and S. Mondal, “A New Strategy For The Synthesis Of Coumarinand Quinolone-Annulated Pyrroles via Pd(0)-Mediated Cross Coupling Followed by Cu(I)-Catalyzed Heteroannulation,” Tetrahedron Letters, Vol. 49, No. 15, 2008, pp. 2418-2420. doi:10.1016/j.tetlet.2008.02.044

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.