Friedlӓnder's synthesis of quinolines as a pivotal step in the development of bioactive heterocyclic derivatives in the current era of medicinal chemistry.
- Published in:
- 2022
- By:
- Publication type:
- Literature Review
Works matching AU Satheeshkumar, Rajendran
Results: 15
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Synthesis of 2‐aminobenzophenone‐based Schiff base Pd(II) complexes: Investigation on crystal structure, biological behavior of DNA/protein‐binding, molecular docking, and in vitro anticancer activities.
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- Applied Organometallic Chemistry, 2020, v. 34, n. 10, p. 1, doi. 10.1002/aoc.5856
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- Publication type:
- Article
3
Synthesis, In Vitro Cytotoxicity, and DFT Studies of Novel 2‐Amino Substituted Benzonaphthyridines as PDK1 Inhibitors.
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- ChemistrySelect, 2022, v. 7, n. 13, p. 1, doi. 10.1002/slct.202200288
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- Publication type:
- Article
4
Solvent‐Free Synthesis of New Quinoline Derivatives via Eaton's Reagent Catalysed Friedländer Synthesis.
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- ChemistrySelect, 2022, v. 7, n. 7, p. 1, doi. 10.1002/slct.202104416
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- Publication type:
- Article
5
Synthesis and Cytotoxicity of Novel Indoloquinolines and Benzonaphthyridines from 4‐Chloro‐2,8‐dimethylquinoline and Variety of Hetero Amines.
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- ChemistrySelect, 2021, v. 6, n. 28, p. 7136, doi. 10.1002/slct.202101269
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- Publication type:
- Article
6
Synthesis of Novel Quin[1,2-b]Acridines: In Vitro Cytotoxicity and Molecular Docking Studies.
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- Polycyclic Aromatic Compounds, 2021, v. 41, n. 8, p. 1631, doi. 10.1080/10406638.2019.1689515
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- Publication type:
- Article
7
Friedländer Synthesis of Novel Polycyclic Quinolines Using Solid SiO<sub>2</sub>/H<sub>2</sub>SO<sub>4</sub> Catalyst.
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- Organic Preparations & Procedures International, 2021, v. 53, n. 2, p. 138, doi. 10.1080/00304948.2020.1865069
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- Publication type:
- Article
8
Convergent synthesis, drug target prediction, and docking studies of new 2,6,9‐trisubstituted purine derivatives.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 97, doi. 10.1002/jhet.4368
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- Publication type:
- Article
9
Synthesis of novel benzo naphtho naphthyridines from 2,4‐dicloroquinolines.
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- Journal of Heterocyclic Chemistry, 2021, v. 58, n. 9, p. 1809, doi. 10.1002/jhet.4312
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- Publication type:
- Article
10
Targeting Allosteric Site of PCSK9 Enzyme for the Identification of Small Molecule Inhibitors: An In Silico Drug Repurposing Study.
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- Biomedicines, 2024, v. 12, n. 2, p. 286, doi. 10.3390/biomedicines12020286
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- Publication type:
- Article
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Synthesis of heteroannulated cyclopent[ b ]indoles: Exploration of in vitro cytotoxicity and molecular docking studies.
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- Synthetic Communications, 2018, v. 48, n. 4, p. 447, doi. 10.1080/00397911.2017.1407792
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- Publication type:
- Article
12
Indium triflate and ionic liquid-mediated Friedländer synthesis of 2-acylquinolines.
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- Synthetic Communications, 2017, v. 47, n. 21, p. 1940, doi. 10.1080/00397911.2017.1357185
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- Publication type:
- Article
13
Solvent-free synthesis of dibenzo[ b,j ][1,10]phenanthroline derivatives using Eaton’s reagent as catalyst.
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- Synthetic Communications, 2017, v. 47, n. 10, p. 990, doi. 10.1080/00397911.2017.1301480
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- Publication type:
- Article
14
Efficient novel synthesis of pyrano[3,2- a ]- and pyrazolo[4,3- a ]-acridines.
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- Synthetic Communications, 2017, v. 47, n. 3, p. 245, doi. 10.1080/00397911.2016.1262038
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- Publication type:
- Article
15
Efficient Protocol for Synthesis of Pyrazolo[3,4- a ]acridines.
- Published in:
- Synthetic Communications, 2015, v. 45, n. 19, p. 2203, doi. 10.1080/00397911.2015.1070433
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- Publication type:
- Article