99867-16-0Relevant academic research and scientific papers
Copper-Catalyzed Aza-Michael Addition of 2-Aminobenzoate to β-Substituted α,β-Unsaturated Ketones: One-Pot Synthesis of 3-Carbonyl-2-Substituted Quinolin-4(1H)-ones
Kang, Seongil,Park, Subin,Kim, Kyung-Su,Song, Changsik,Lee, Yunmi
, p. 2694 - 2705 (2018/03/09)
We present a new and straightforward one-pot process for the synthesis of 3-carbonyl-4-quinolone derivatives through highly efficient Cu-catalyzed aza-Michael addition of 2-aminobenzoates to β-substituted α,β-unsaturated ketones/cyclization/mild oxidation
Microwave assisted gould-jacobs reaction for synthesis of 3-acetyl-4-hydroxyquinoline derivatives
Uz Zaman, Ashhar,Ain Khan, Misbahul,Ali Munawar, Munawar,Athar, Muhammad Makshoof,Pervaiz, Muhammad,Pervaiz, Ansar,Mahmood, Ayaz
, p. 2823 - 2826 (2015/12/11)
Different types of quinoline derivatives have been synthesized by microwave irradiation and reaction yields were compared with reported classical methodology. The emphasis on this research project was to reduce reaction times and enhance the yields of the
QUINOLINE DERIVATIVES AND MELK INHIBITORS CONTAINING THE SAME
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Page/Page column 261-262, (2012/02/13)
The present invention directs a compound represented by formula (I).
Structural and theoretical studies of [6-bromo-1-(4-fluorophenylmethyl)-4(1H)-quinolinon-3-yl)]-4-hydroxy-2-oxo-3-butenoic acid as HIV-1 integrase inhibitor
Vandurm, Pierre,Cauvin, Christine,Guiguen, Allan,Georges, Benoit,Van, Kiet Le,Martinelli, Valerie,Cardona, Christelle,Mbemba, Gladys,Mouscadet, Jean-Francois,Hevesi, Laszlo,Lint, Carine Van,Wouters, Johan
supporting information; scheme or table, p. 4806 - 4809 (2010/04/28)
Ethyl [6-bromo-1-(4-fluorophenylmethyl)-4(1H)-quinolinon-3-yl]-4-hydroxy-2-oxo-3-butenoate 1 and [6-bromo-1-(4-fluorophenylmethyl)-4(1H)-quinolinon-3-yl)]-4-hydroxy-2-oxo-3-butenoic acid 2 were synthesized as potential HIV-1 integrase inhibitors and evalu
