Literature DB >> 24125098

Employing arynes in transition-metal-free monoarylation of aromatic tertiary amines.

Sachin Suresh Bhojgude1, Trinadh Kaicharla, Akkattu T Biju.   

Abstract

The highly monoselective N-arylation of aromatic tertiary amines using a transition-metal-free approach using arynes has been developed. The reaction afforded functionalized diaryl amines in moderate to excellent yield. High levels of functional group compatibility especially with halogen containing substrates, dyes and donor-acceptor systems, and high yields of products are the notable features of the present reaction.

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Year:  2013        PMID: 24125098     DOI: 10.1021/ol4029258

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Mechanistic Duality in Tertiary Amine Additions to Thermally Generated Hexadehydro-Diels-Alder Benzynes.

Authors:  Sean P Ross; Beeraiah Baire; Thomas R Hoye
Journal:  Org Lett       Date:  2017-10-05       Impact factor: 6.005

Review 2.  Uncovering the Neglected Similarities of Arynes and Donor-Acceptor Cyclopropanes.

Authors:  Daniel B Werz; Akkattu T Biju
Journal:  Angew Chem Int Ed Engl       Date:  2019-12-12       Impact factor: 15.336

  2 in total

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