Literature DB >> 26902665

N-Arylation of Tertiary Amines under Mild Conditions.

Maayan Hirsch1, Shubhendu Dhara1, Charles E Diesendruck1.   

Abstract

A transition-metal-free procedure for the N-arylation of tertiary amines to sp(3) quaternary ammonium salts is described. The presented conditions allow for the isolation of trialkylaryl, dialkyldiaryl, and novel triarylalkyl ammonium salts, including N-chiral quaternary ammonium salts. The reaction works at room temperature, open to air with electron-rich or -poor benzyne precursors and different tertiary amines, allowing the synthesis of a broad range of N-aryl ammonium salts that have applications in a variety of fields.

Entities:  

Year:  2016        PMID: 26902665     DOI: 10.1021/acs.orglett.6b00078

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


  3 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

2.  Synthesis and characterization of tetraphenylammonium salts.

Authors:  Hikaru Fujita; Ozora Sasamoto; Shiori Kobayashi; Masanori Kitamura; Munetaka Kunishima
Journal:  Nat Commun       Date:  2022-05-09       Impact factor: 17.694

3.  Increasing the Alkaline Stability of N,N-Diaryl Carbazolium Salts Using Substituent Electronic Effects.

Authors:  Nansi Gjineci; Sinai Aharonovich; Dario R Dekel; Charles E Diesendruck
Journal:  ACS Appl Mater Interfaces       Date:  2020-10-22       Impact factor: 9.229

  3 in total

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