New 2-(aryl/heteroaryl)-6-(morpholin-4-yl/pyrrolidin-1-yl)-(4-trifluoromethyl)quinolines: synthesis via Buchwald–Hartwig amination, photophysics, and biomolecular binding properties-Reference-Cited by-同舟云学术

New 2-(aryl/heteroaryl)-6-(morpholin-4-yl/pyrrolidin-1-yl)-(4-trifluoromethyl)quinolines: synthesis via Buchwald–Hartwig amination, photophysics, and biomolecular binding properties

Published:2018 Issue:12 Volume:42 Page:10024-10035
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Bonacorso Helio G.¹²³⁴⁵^ORCID,Rodrigues Melissa B.¹²³⁴⁵,Iglesias Bernardo A.²³⁴⁵^ORCID,da Silveira Carolina H.²³⁴⁵,Feitosa Sarah C.¹²³⁴⁵,Rosa Wilian C.¹²³⁴⁵,Martins Marcos A. P.¹²³⁴⁵^ORCID,Frizzo Clarissa P.¹²³⁴⁵^ORCID,Zanatta Nilo¹²³⁴⁵^ORCID

Affiliation:

1. Núcleo de Química de Heterociclos (NUQUIMHE)

2. Departamento de Química

3. Universidade Federal de Santa Maria

4. Santa Maria

5. Brazil

Abstract

New 6-(morpholino/pyrrolidino)quinolines displaying interesting photophysical and biomolecular binding properties achieved by Buchwald–Hartwig amination.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/NJ/C8NJ01120F

Reference45 articles.

1. Quinolone antibacterial agents. Synthesis and structure-activity relationships of 8-substituted quinoline-3-carboxylic acids and 1,8-naphthyridine-3-carboxylic acids