Unusual open chain quinolinyl peroxol and its alcohol counterpart obtained through a modified Skraup-Doebner-Von Miller quinoline synthesis: theoretical studies and complete 1H- and 13C-NMR assignments-Reference-Cited by-同舟云学术

Unusual open chain quinolinyl peroxol and its alcohol counterpart obtained through a modified Skraup-Doebner-Von Miller quinoline synthesis: theoretical studies and complete 1H- and 13C-NMR assignments

Published:2012-01 Issue:1 Volume:50 Page:68-73
ISSN:0749-1581
Container-title:Magnetic Resonance in Chemistry
language:en
Short-container-title:Magn. Reson. Chem.

Author:

Fotie Jean¹,Kemami Wangun Hilaire V.²,Dreux Katelyn¹,Sommerfeld Thomas¹,Pittman Jacob¹

Affiliation:

1. Department of Chemistry and Physics; Southeastern Louisiana University; Hammond; LA; USA

2. Harbor Branch Oceanographic Institute, Centre of Marine Biomedical and Biotechnology Research; Florida Atlantic University; Fort Pierce; FL; USA

Publisher

Wiley

Subject

General Materials Science,General Chemistry

Reference14 articles.

1. Key Natural Products in Malaria Chemotherapy: From Quinine to Artemisinin and Beyond

2. Synthesis, antioxidant and toxicological study of novel pyrimido quinoline derivatives from 4-hydroxy-3-acyl quinolin-2-one

3. Synthesis and Pharmacological Evaluation of Some 4-Oxo-quinoline-2-carboxylic Acid Derivatives as Anti-inflammatory and Analgesic Agents

4. Discovery of Indeno[1,2-c]quinoline Derivatives as Inhibitors of Osteoclastogenesis Induced by Receptor Activator of NF-κB Ligand (RANKL)

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