Literature DB >> 22038250

Synthesis of novel 2,8-disubstituted indolo[3,2-b]carbazoles.

Sven Van Snick1, Wim Dehaen.   

Abstract

A new synthetic pathway towards 2,8-difunctionalised indolo[3,2-b]carbazoles was investigated. The presented method offers a short and high yielding route towards 2,8-dibromo-5,11-dihexyl-6,12-diphenyl-indolo[3,2-b]carbazole. It is demonstrated that the latter compound is a versatile building block, enabling the synthesis of a number of previously unreported 5,11-dialkyl-6,12-diphenyl-indolo[3,2-b]carbazoles in moderate to good yields, using Suzuki and Sonogashira cross-coupling reaction. Furthermore it is shown that 2,8-dibromo-5,11-dihexyl-6,12-diphenyl-indolo[3,2-b]carbazole can be easily formylated, giving rise to the 2,8-diformyl-5,11-dihexyl-6,12-diphenyl-indolo-[3,2-b]carbazole. The latter compound was successfully subjected to condensation reactions.

Entities:  

Year:  2011        PMID: 22038250     DOI: 10.1039/c1ob06298k

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


  2 in total

1.  Nitration of 5,11-dihydroindolo[3,2-b]carbazoles and synthetic applications of their nitro-substituted derivatives.

Authors:  Roman A Irgashev; Nikita A Kazin; Gennady L Rusinov; Valery N Charushin
Journal:  Beilstein J Org Chem       Date:  2017-07-14       Impact factor: 2.883

Review 2.  Synthesis of Linearly Fused Benzodipyrrole Based Organic Materials.

Authors:  Maarten Vlasselaer; Wim Dehaen
Journal:  Molecules       Date:  2016-06-17       Impact factor: 4.411

  2 in total

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