Convenient and efficient method for the synthesis of substituted quinolines via one-pot heteroannulation reaction of o-amino arylketones with α-methylene ketones under solvent-free conditions
Author:
Affiliation:
1. Department of Chemistry, Osmania University, Tarnaka, Hyderabad, India
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2016.1242746
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1. Practical Route to a New Class of LTD4 Receptor Antagonists
2. Synthesis and pharmacological properties of some quinoline derivatives
3. A New Series of PDGF Receptor Tyrosine Kinase Inhibitors: 3-Substituted Quinoline Derivatives
4. New benzo[5,6]pyrrolizino[1,2- b ]quinolines as cytotoxic agents
5. Plant Antitumor Agents. I. The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca acuminata1,2
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3. Environmentally Friendly Nafion-Mediated Friedländer Quinoline Synthesis under Microwave Irradiation: Application to One-Pot Synthesis of Substituted Quinolinyl Chalcones;Synthesis;2020-03-19
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