Literature DB >> 24164294

Visible-light-mediated nucleophilic addition of an α-aminoalkyl radical to isocyanate or isothiocyanate.

Hongxia Zhou1, Ping Lu, Xiangyong Gu, Pixu Li.   

Abstract

A visible-light photoredox synthesis of α-amino amide or α-amino thioamide from N,N-dimethylaniline derivatives and aryl isocyanate or aryl isothiocyanate was developed. Bis[2-(4,6-difluorophenyl)pyridinato-C(2),N](picolinato)iridium(III) (FIrpic) was found to be the effective catalyst among six catalysts screened. The reaction involves generation of α-aminoalkyl radicals from tertiary amines, followed by radical addition to the electron-deficient carbon of isocyanate and isothiocyanate.

Entities:  

Year:  2013        PMID: 24164294     DOI: 10.1021/ol402573j

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


  4 in total

Review 1.  Recent Advances in Photoredox-Mediated Radical Conjugate Addition Reactions: An Expanding Toolkit for the Giese Reaction.

Authors:  Anastasia L Gant Kanegusuku; Jennifer L Roizen
Journal:  Angew Chem Int Ed Engl       Date:  2021-07-21       Impact factor: 16.823

2.  Photoredox catalysis in a complex pharmaceutical setting: toward the preparation of JAK2 inhibitor LY2784544.

Authors:  James J Douglas; Kevin P Cole; Corey R J Stephenson
Journal:  J Org Chem       Date:  2014-11-17       Impact factor: 4.354

3.  Photoredox α-vinylation of α-amino acids and N-aryl amines.

Authors:  Adam Noble; David W C MacMillan
Journal:  J Am Chem Soc       Date:  2014-08-11       Impact factor: 15.419

Review 4.  Recent Advances in Visible-Light-Mediated Amide Synthesis.

Authors:  Bin Lu; Wen-Jing Xiao; Jia-Rong Chen
Journal:  Molecules       Date:  2022-01-14       Impact factor: 4.411

  4 in total

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