Literature DB >> 22105760

Regioselective C-H bond functionalizations of acridines using organozinc reagents.

Isao Hyodo1, Mamoru Tobisu, Naoto Chatani.   

Abstract

Despite the recent advance in C-H bond functionalization chemistry, the C-H bonds in the acridine ring system, which is an important scaffold in medicinal and material science, have met with limited success, due, in part, to the lack of activated C-H bonds adjacent to the ring nitrogen atom. Herein, several protocols that can effect the regioselective arylation and alkylation of acridines at the C-4 and C-9 positions are described. This journal is © The Royal Society of Chemistry 2012

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Year:  2011        PMID: 22105760     DOI: 10.1039/c1cc16582h

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Facile synthesis of unsymmetrical acridines and phenazines by a Rh(III)-catalyzed amination/cyclization/aromatization cascade.

Authors:  Yajing Lian; Joshua R Hummel; Robert G Bergman; Jonathan A Ellman
Journal:  J Am Chem Soc       Date:  2013-08-19       Impact factor: 15.419

2.  Synthesis of Acridines through Alkyne Addition to Diarylamines.

Authors:  Kristen E Berger; Grant M McCormick; Joseph A Jaye; Christina M Rozeske; Eric H Fort
Journal:  Molecules       Date:  2018-11-03       Impact factor: 4.411

  2 in total

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