Abstract
A new, efficient and green methodology for obtaining quinolines based on the use of tungstophosphoric acid included in a polymeric matrix of polyacrylamide is proposed (APTPOL60). The methodology involves the formation of polysubstituted quinoline compounds using a variety of 2-aminoaryl ketones and β-dicarbonyl compounds, in absolute ethanol as reaction solvent, and a temperature of 78 ºC. The catalyst efficiency is not compromised after its successive use in reactions, and no leaching was observed. Seven examples of quinolone derivatives were obtained with excellent yields (89%–99%). This is the first report about the use of a heteropolyacid included in a polymeric matrix as recyclable catalyst in the Friedlander synthesis of quinoline derivatives (molecules with biological activity potential).
Keywords: Quinolines, friedlander synthesis, tungstophosphoric acid, polymeric matrix, heterogeneous catalysts.
Graphical Abstract
Current Catalysis
Title:An Efficient and Green Catalytic Method for Friedländer Quinoline Synthesis Using Tungstophosphoric Acid Included in a Polymeric Matrix
Volume: 4 Issue: 1
Author(s): Daniel O. Bennardi, Mirta N. Blanco, Luis R. Pizzio, Juan C. Autino and Gustavo P. Romanelli
Affiliation:
Keywords: Quinolines, friedlander synthesis, tungstophosphoric acid, polymeric matrix, heterogeneous catalysts.
Abstract: A new, efficient and green methodology for obtaining quinolines based on the use of tungstophosphoric acid included in a polymeric matrix of polyacrylamide is proposed (APTPOL60). The methodology involves the formation of polysubstituted quinoline compounds using a variety of 2-aminoaryl ketones and β-dicarbonyl compounds, in absolute ethanol as reaction solvent, and a temperature of 78 ºC. The catalyst efficiency is not compromised after its successive use in reactions, and no leaching was observed. Seven examples of quinolone derivatives were obtained with excellent yields (89%–99%). This is the first report about the use of a heteropolyacid included in a polymeric matrix as recyclable catalyst in the Friedlander synthesis of quinoline derivatives (molecules with biological activity potential).
Export Options
About this article
Cite this article as:
O. Bennardi Daniel, N. Blanco Mirta, R. Pizzio Luis, C. Autino Juan and P. Romanelli Gustavo, An Efficient and Green Catalytic Method for Friedländer Quinoline Synthesis Using Tungstophosphoric Acid Included in a Polymeric Matrix, Current Catalysis 2015; 4 (1) . https://dx.doi.org/10.2174/2211544704666150424234036
DOI https://dx.doi.org/10.2174/2211544704666150424234036 |
Print ISSN 2211-5447 |
Publisher Name Bentham Science Publisher |
Online ISSN 2211-5455 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
- Announcements
Related Articles
-
23Na Magnetic Resonance Imaging for the Determination of Myocardial Viability: The Status and the Challenges
Current Vascular Pharmacology Sleep Disordered Breathing: Alternatives to CPAP Therapy
Current Respiratory Medicine Reviews Alzheimer Disease and Type 2 Diabetes Mellitus: The Link to Tyrosine Hydroxylase and Probable Nutritional Strategies
CNS & Neurological Disorders - Drug Targets Clinical Uses of 1-alpha-hydroxycholecalciferol
Current Vascular Pharmacology Cardiovascular Disease Risk of Type 2 Diabetes Mellitus and Metabolic Syndrome: Focus on Aggressive Management of Dyslipidemia
Current Diabetes Reviews The Genetics of Small-Vessel Disease
Current Medicinal Chemistry Assessing The Treatment Effect in Metabolic Syndrome Without Perceptible Diabetes (ATTEMPT): A Prospective-Randomized Study in Middle Aged Men and Women
Current Vascular Pharmacology Hypothyroidism and Cardiovascular Disease: Factors, Mechanism and Future Perspectives
Current Medicinal Chemistry The Glucocorticoid Receptor: Molecular Mechanism and New Therapeutic Opportunities
Current Drug Targets - Inflammation & Allergy Small Artery Remodeling in Obesity and Insulin Resistance
Current Vascular Pharmacology Models to Study Atherosclerosis: A Mechanistic Insight
Current Vascular Pharmacology Intestinal Microbiota: A Regulator of Intestinal Inflammation and Cardiac Ischemia?
Current Drug Targets Effects of Thiazolidinediones Beyond Glycaemic Control
Current Pharmaceutical Design Cardiovascular Manifestations of COVID-19
Current Cardiology Reviews Transient Focal Lesions in the Splenium of the Corpus Callosum with Restricted Diffusion: An Enigma
Current Medical Imaging To Be-et, or Not to Be-et, That is the Question: The Role(s) of Nitrate and Nitrite in Health and Illness
Reviews on Recent Clinical Trials Cellular and Pharmacological Targets to Induce Coronary Arteriogenesis
Current Cardiology Reviews Oxidative Stress and Endothelial Dysfunction in Cardiovascular Disease: Mitochondria-Targeted Therapeutics
Current Medicinal Chemistry Is the Vascular System a Main Target for Thyroid Hormones? From Molecular and Biochemical Findings to Clinical Perspectives
Current Vascular Pharmacology Green Tea from the Far East to the Drug Store: Focus on the Beneficial Cardiovascular Effects
Current Pharmaceutical Design