One-pot synthesis of 2,3-bis-(4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)succinates and arylmethylene-bis-3,3′-quinoline-2-ones-Reference-Cited by-同舟云学术

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One-pot synthesis of 2,3-bis-(4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)succinates and arylmethylene-bis-3,3′-quinoline-2-ones

Published:2018-07-30 Issue:1 Volume:73 Page:27-37
ISSN:2585-7290
Container-title:Chemical Papers
language:en
Short-container-title:Chem. Pap.

Author:

Aly Ashraf A.,El-Sheref Essmat M.,Mourad Aboul-Fetouh E.,Bakheet Momtaz E. M.,Bräse Stefan,Nieger Martin

Publisher

Springer Science and Business Media LLC

Subject

Materials Chemistry,Industrial and Manufacturing Engineering,General Chemical Engineering,Biochemistry,General Chemistry

Link

http://link.springer.com/article/10.1007/s11696-018-0561-0/fulltext.html

Reference28 articles.

1. Abass M, Mostafa BB (2005) Synthesis and evaluation of molluscicidal and larvicidal activities of some novel enaminones derived from 4-hydroxyquinolinones: part IX. Bioorg Med Chem 13:6133–6144. https://doi.org/10.1016/j.bmc.2005.06.038

2. Abass M, Hassanin HM, Allimony HA, Hassan H (2015) Substituted quinolinones 27. Regioselective synthesis of pyrazolo-, oxazolo-, and triazepinoquinoline derivatives. Chem Heterocycl Compd 51:1023–1029. https://doi.org/10.1007/s10593-016-1813-y

3. Ahmed N, Brahmbhatt KG, Sabde S, Mitra D, Singh IP, Bhutani KK (2010) Synthesis and anti-HIV activity of alkylated quinoline 2,4-diols. Bioorg Med Chem 18:2872–2879. https://doi.org/10.1016/j.bmc.2010.03.015

4. Al-Trawneh SA, Zahra JA, Kamal MR, El-Abadelah MM, Zani F, Incerti M, Cavazzoni A, Alfieri RR, Petronini PG, Vicini P (2010) Synthesis and biological evaluation of tetracyclic fluoroquinolones as antibacterial and anticancer agents. Bioorg Med Chem 18:5873–5884. https://doi.org/10.1016/j.bmc.2010.06.098

5. Aly AA, El-Sheref EM, Mourad Aboul-Fetouh E, Brown AB, Bräse S, Bakheet ME, Nieger M (2018) Synthesis of spiro[indoline-3,4′-pyrano[3,2-c]quinolone]-3′-carbonitriles. Monatsh Chem 149(149):635–644. https://doi.org/10.1007/s00706-017-2078-6

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