Şengül, İbrahim FazılSomphol, KittiyaKandemir, HakanKumar, NareshBlack, David StC.2022-05-112022-05-1120140040-4020https://doi.org/10.1016/j.tet.2014.11.014https://hdl.handle.net/20.500.11776/71763,6-Bis-(2-indolyl)dibenzofurans 1,2, and carbazoles 3-6 underwent a range of electrophilic substitution reactions to produce formyl indoles 7-12, biindolyls 24-28 and 33-34, glyoxylamides 40-42, and amides 48. (C) 2014 Elsevier Ltd. All rights reserved.en10.1016/j.tet.2014.11.014info:eu-repo/semantics/closedAccessBis-indolesBiindolylsDibenzofuransCarbazolesIndole synthesisFormylationGlyoxylic amidesElectrophilic substitutionSolid-State StructuresMacrocyclic AmideComplexes4,6-DimethoxyindolesBiindolylsChlorideIndolesSome electrophilic reactivity studies of di-(2-indolyl)dibenzofurans and di-(2-indolyl)carbazolesArticle705196019614Q2WOS:0003471279000042-s2.0-84911869349Q2