Literature DB >> 23168677

Synthesis of phenanthridinones via palladium-catalyzed C(sp2)-H aminocarbonylation of unprotected o-arylanilines.

Dongdong Liang1, Ziwei Hu, Jiangling Peng, Jinbo Huang, Qiang Zhu.   

Abstract

An efficient synthesis of free (NH)-phenanthridinones through Pd-catalyzed C(sp(2))-H aminocarbonylation of unprotected o-arylanilines under an atmospheric pressure of CO has been developed. Some ortho heteroarene substituted anilines as well as N-alkyl protected o-arylanilines are also suitable substrates for this C-H aminocarbonylation reaction.

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Year:  2012        PMID: 23168677     DOI: 10.1039/c2cc36817j

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


  3 in total

1.  Reversed reactivity of anilines with alkynes in the rhodium-catalysed C-H activation/carbonylation tandem.

Authors:  Siba P Midya; Manoj K Sahoo; Vinod G Landge; P R Rajamohanan; Ekambaram Balaraman
Journal:  Nat Commun       Date:  2015-10-21       Impact factor: 14.919

2.  Pd-catalyzed dehydrogenative annulation approach for the efficient synthesis of phenanthridinones.

Authors:  Xinyao Li; Jun Pan; Song Song; Ning Jiao
Journal:  Chem Sci       Date:  2016-04-26       Impact factor: 9.825

3.  Weak Base-Promoted Lactamization under Microwave Irradiation: Synthesis of Quinolin-2(1H)-ones and Phenanthridin-6(5H)-ones.

Authors:  Pham Duy Quang Dao; Ho-Jin Lim; Chan Sik Cho
Journal:  ACS Omega       Date:  2018-09-27
  3 in total

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