Convenient Synthesis of C-2 Substituted 1,3-Azoles and Other Related N-Heterocyclic Derivatives via Base and Iodine-Mediated Carbon-Hydrogen (C-H) Bond Functionalization
(1)To transform a carbon-hydrogen (C-H) bond at C-2 position of unfunctionalized 1,3-azoles and other related heterocyclic precursors to a carbon-heteroatom bond (C-Y; Y = N, O, S) via base and iodine-mediated bond formation
(2) To develop a convenient, air-stable and versatile one-pot reaction methodology for the synthesis of various heterocyclic derivatives
(3) To investigate a mechanism of this reaction and understand a role of each reagent
