Your browser doesn't support javascript.
loading
Synthesis of Symmetric Bis(N-alkylaniline)triarylmethanes via Friedel-Crafts-Catalyzed Reaction between Secondary Anilines and Aldehydes.
Gomes, Rafael F A; Coelho, Jaime A S; Frade, Raquel F M; Trindade, Alexandre F; Afonso, Carlos A M.
Afiliação
  • Gomes RF; Instituto de Investigação do Medicamento (iMed.ULisboa), Faculty of Pharmacy, University of Lisbon , Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal.
  • Coelho JA; Instituto de Investigação do Medicamento (iMed.ULisboa), Faculty of Pharmacy, University of Lisbon , Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal.
  • Frade RF; Instituto de Investigação do Medicamento (iMed.ULisboa), Faculty of Pharmacy, University of Lisbon , Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal.
  • Trindade AF; Instituto de Investigação do Medicamento (iMed.ULisboa), Faculty of Pharmacy, University of Lisbon , Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal.
  • Afonso CA; Instituto de Investigação do Medicamento (iMed.ULisboa), Faculty of Pharmacy, University of Lisbon , Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal.
J Org Chem ; 80(20): 10404-11, 2015 Oct 16.
Article em En | MEDLINE | ID: mdl-26402221
The first general protocol for the preparation of symmetric triarylmethanes bearing secondary anilines by ytterbium-catalyzed Friedel-Crafts reaction of hetero(aryl) aldehydes and secondary anilines is reported. Mechanistic studies indicated that the iminium ion intermediate is the electrophilic partner. The reaction is greatly accelerated by high pressure (9 kbar) and showed a broad substrate scope on the hetero(aryl) aldehyde. The new triarylmethanes exhibited activity against HT-29 cancer cell lines, with the best result scoring an IC50 of 1.74 µM.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article