Jump to main content
Jump to site search

Issue 18, 2018
Previous Article Next Article

Synthesis of thieno[2,3-c]acridine and furo[2,3-c]acridine derivatives via an iodocyclization reaction and their fluorescence properties and DFT mechanistic studies

Author affiliations

Abstract

In this paper, we report the novel synthesis of thieno[2,3-c]acridine and furo[2,3-c]acridine derivatives via an intramolecular iodocyclization reaction. The thieno[2,3-c]acridine derivatives exhibited blue fluorescence in hexane. DFT and time-dependent (TD) DFT studies were carried out. This methodology provided a novel pathway to access thieno[2,3-c]acridine and furo[2,3-c]acridine derivatives via a 6-endo iodocyclization reaction.

Graphical abstract: Synthesis of thieno[2,3-c]acridine and furo[2,3-c]acridine derivatives via an iodocyclization reaction and their fluorescence properties and DFT mechanistic studies

Back to tab navigation

Supplementary files

Publication details

The article was received on 14 Jul 2018, accepted on 10 Aug 2018 and first published on 10 Aug 2018


Article type: Paper
DOI: 10.1039/C8NJ03511C
Citation: New J. Chem., 2018,42, 15315-15324
  •   Request permissions

    Synthesis of thieno[2,3-c]acridine and furo[2,3-c]acridine derivatives via an iodocyclization reaction and their fluorescence properties and DFT mechanistic studies

    A. D. Sonawane, D. R. Garud, T. Udagawa, Y. Kubota and M. Koketsu, New J. Chem., 2018, 42, 15315
    DOI: 10.1039/C8NJ03511C

Search articles by author

Spotlight

Advertisements