Green and fast 2-aryloxylation/amination of quinolines-Reference-Cited by-同舟云学术

Green and fast 2-aryloxylation/amination of quinolines

Published:2024 Issue:8 Volume:26 Page:4659-4664
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Bu Changna¹,Wang Kaijuan¹,Gong Chengcheng¹,Wang Dong¹²^ORCID

Affiliation:

1. State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources, College of Chemistry, Xinjiang University, Urumqi 830017, Xinjiang, China

2. Institute of Materia Medica, Xinjiang University, Urumqi 830017, Xinjiang, China

Abstract

The direct C2-H functionalization of quinolines has always been a widely concerned area. Herein we report a rapid and eco-friendly synthesis of 2-aroxyquinolines and 2-aminoquinolines through deoxygenative functionalization of quinoline N-oxides.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/GC/D3GC05178A

Reference49 articles.

1. A directing group-assisted ruthenium-catalyzed approach to access meta-nitrated phenols

2. Chelation-assisted de-aryloxylative amination of 2-aryloxy quinolines: a new synthetic route to a key fragment of a bioactive PRMT5 inhibitor

3. Synthesis, Structure−Activity Relationship, and Receptor Pharmacology of a New Series of Quinoline Derivatives Acting as Selective, Noncompetitive mGlu1 Antagonists

4. II. Synthesis and Biological Evaluation of Some Bioisosteres and Congeners of the Antitumor Agent, 2-{4-[(7-Chloro-2-quinoxalinyl)oxy]phenoxy}propionic Acid (XK469)

5. Design, synthesis, biological evaluation and molecular modelling studies of novel quinoline derivatives against Mycobacterium tuberculosis

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