Literature DB >> 19109685

A facile and general method for the synthesis of 6,12-diaryl-5,11-dihydroindolo[3,2-b]carbazoles.

Rong Gu1, Sven Van Snick, Koen Robeyns, Luc Van Meervelt, Wim Dehaen.   

Abstract

A facile and general two-step method towards 6,12-diaryl-5,11-dihydroindolo[3,2-b]carbazoles has been developed. Hydroiodic acid was an efficient catalyst for the condensation of indole and aromatic aldehydes, and iodine was used as an oxidation reagent to afford symmetrical 6,12-diaryl-5,11-dihydroindolo[3,2-b]carbazoles in moderate to good overall yields.

Entities:  

Year:  2008        PMID： 19109685     DOI： 10.1039/b815908d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN： 1477-0520            Impact factor:   3.876


  2 in total

1.  Synthesis and characterization of novel donor-acceptor type neutral green electrochromic polymers containing an indolo[3,2-b]carbazole donor and diketopyrrolopyrrole acceptor.

Authors:  Yan Zhang; Lingqian Kong; Xiuping Ju; Hongmei Du; Jinsheng Zhao; Yu Xie
Journal:  RSC Adv       Date:  2018-06-11       Impact factor: 4.036

2.  5',11'-Dihydro-dispiro-[cyclo-hexane-1,6'-indolo[3,2-b]carbazole-12',1''-cyclo-hexa-ne].

Authors:  Ilia A Guzei; Lara C Spencer; Eric Codner; Joshua M Boehm
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-12-03
  2 in total

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