The remarkable selectivity of the 2-arylquinoline-based acyl hydrazones toward copper salts: exploration of their catalytic applications in the copper catalysed N-arylation of indole derivatives and C1-alkynylation of tetrahydroisoquinolines via the A3 reaction-Reference-Cited by-同舟云学术

The remarkable selectivity of the 2-arylquinoline-based acyl hydrazones toward copper salts: exploration of their catalytic applications in the copper catalysed N-arylation of indole derivatives and C1-alkynylation of tetrahydroisoquinolines via the A3 reaction

Published:2021 Issue:1 Volume:45 Page:243-250
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Echeverry-Gonzalez Carlos A.¹²³^ORCID,Ortiz Villamizar Marlyn Catalina¹²³^ORCID,Kouznetsov Vladimir V.¹²³^ORCID

Affiliation:

1. Laboratorio de Química Orgánica y Biomolecular, CMN, Universidad Industrial de Santander, Parque Tecnológico Guatiguará

2. Piedecuesta

3. Colombia

Abstract

Different selective 2-arylquinoline-based acyl hydrazones toward copper(i) salts were synthesised, characterized and studied their applicability as metal ligands in diverse chemical transformations.

Funder

Departamento Administrativo de Ciencia, Tecnología e Innovación

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2021/NJ/D0NJ04516K

Reference53 articles.

1. Stereoselective, solvent free, highly efficient synthesis of aldo- and keto-N-acylhydrazones applying grindstone chemistry

2. A review on quinoline hydrazone derivatives as a new class of potent antitubercular and anticancer agents

3. Acylhydrazones as Widely Tunable Photoswitches