Literature DB >> 21250705

Ligand-free copper-catalyzed arylation of amidines.

Michelle Cortes-Salva1, Corey Garvin, Jon C Antilla.   

Abstract

Copper-catalyzed cross-coupling reactions of amidine salts were utilized to synthesize monoarylated amidines in moderate to high yields with ligand-free conditions. DMF was the superior solvent for the N-arylation of benzamidines, while MeCN was used in the formation of N-aryl amidines in moderate to high yield.

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Year:  2011        PMID: 21250705     DOI: 10.1021/jo102235u

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  4 in total

1.  Palladium-catalyzed N-monoarylation of amidines and a one-pot synthesis of quinazoline derivatives.

Authors:  Meredeth A McGowan; Camille Z McAvoy; Stephen L Buchwald
Journal:  Org Lett       Date:  2012-07-05       Impact factor: 6.005

2.  RECENT SYNTHETIC DEVELOPMENTS AND APPLICATIONS OF THE ULLMANN REACTION. A REVIEW.

Authors:  Hao Lin; Dianqing Sun
Journal:  Org Prep Proced Int       Date:  2013       Impact factor: 1.628

3.  N-(2-Iodo-phen-yl)benzene-carbox-imid-amide.

Authors:  Yin-Jun Zhang; Dong Wang; Hai-Liang Zhang; Yu-Guang Wang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-02-17

4.  Direct, Late-Stage Mono-N-arylation of Pentamidine: Method Development, Mechanistic Insight, and Expedient Access to Novel Antiparastitics against Diamidine-Resistant Parasites.

Authors:  Jack Robertson; Marzuq A Ungogo; Mustafa M Aldfer; Leandro Lemgruber; Fergus S McWhinnie; Bela E Bode; Katherine L Jones; Allan J B Watson; Harry P de Koning; Glenn A Burley
Journal:  ChemMedChem       Date:  2021-09-02       Impact factor: 3.540

  4 in total

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