13337-57-0Relevant academic research and scientific papers
Regioselective synthesis, antimicrobial evaluation and theoretical studies of 2-styryl quinolines
Kamal, Ahmed,Rahim, Abdul,Riyaz,Poornachandra,Balakrishna, Moku,Kumar, C. Ganesh,Hussaini, Syed Mohammed Ali,Sridhar,Machiraju, Pavan Kumar
, p. 1347 - 1357 (2015)
2-Styryl quinolines (9a-l) have been synthesized regioselectively from 2-methyl-quinoline by using NaOAc in water acetic acid binary solvents and evaluated for their antibacterial activity against both Gram-positive and Gram-negative strains. Among these,
Highly efficient one-pot tandem Friedlander annulation and chemo-selective Csp3-H functionalization under calcium catalysis
Singh, Garima,Yaragorla, Srinivasarao
, p. 18874 - 18882 (2017)
A highly efficient and regioselective Friedlander synthesis of 2-methyl-3-acyl quinolines is described, which occurs under solvent-free conditions and employs calcium triflate as a sustainable catalyst. For the first time in the literature, these 2-methyl
Synthesis of Fe3O4?SiO2/isoniazid/Cu(II) magnetic nanocatalyst as a recyclable catalyst for a highly efficient preparation of quinolines in moderate conditions
Lotfi, Shahram,Nikseresht, Ahmad,Rahimi, Nasrin
, (2019)
This paper reports the investigation on an efficient procedure to prepare Fe3O4?SiO2/isoniazid/Cu(II) as a recoverable magnetic nanocatalyst. The prepared nanocatalyst, Fe3O4?SiO2/isoniazid
Silica sulfuric acid as an inexpensive and recyclable solid acid catalyzed efficient synthesis of quinolines
Shaabani, Ahmad,Soleimani, Ebrahim,Badri, Zahra
, p. 181 - 184 (2006)
Silica sulfuric acid as an inexpensive and recyclable solid acid efficiently catalyzes the Fridedlaender synthesis of quinolines through a condensation reaction of a 2-aminoaryl ketone with an activated α-CH acid compound under solvent-free conditions in
Iodine-catalyzed Friedlander quinoline synthesis under solvent-free conditions
Zolfigol, Mohammad Ali,Salehi, Peyman,Ghaderi, Arash,Shiri, Morteza
, p. 267 - 271 (2007)
Polyfunctional quinolines were synthesized using Friedlander method catalyzed by molecular iodine in high yields at 60 °C under solvent-free conditions.
An efficient solvent-free synthesis of 3-acetyl-4-arylquinoline-based enaminones and its derivatives using DMFDMA reagent
Kumar, L. Jyothish,Vijayakumar
, p. 2001 - 2012 (2018)
Abstract: A series of 3-substituted-4-arylquinoline derivatives were synthesized using 3-acetyl-4-arylquinoline. The acetyl function of 3-acetyl-4-arylquinoline was successfully converted into its corresponding enaminone using DMFDMA as a reagent which in
Design, Synthesis, and Biological Activity of Chalcone Analogs Containing 4-Phenylquinolin and Benzohydrazide
Guan, Li-Ping,He, Li-Ya,He, Zhi-Wen,Liu, Wei-Hua,Tan, Qiu-Wan,Wang, Si-Hong,Zhang, Li,Zhang, Shan-Shan
, (2022/02/01)
A series of chalcone derivatives (3a–3m) containing 4-phenylquinoline and benzohydrazide were designed and synthesized, and their anti-inflammatory, analgesic, and antidepressant activities were evaluated. Using the classic antidepressant model, except fo
Magnetite (Fe3O4) nanoparticles-supported dodecylbenzenesulfonic acid as a highly efficient and green heterogeneous catalyst for the synthesis of substituted quinolines and 1-amidoalkyl-2-naphthol derivatives
Katheriya, Deepak,Patel, Nipun,Dadhania, Harsh,Dadhania, Abhishek
, p. 805 - 816 (2020/10/02)
Abstract: Magnetically retrievable, magnetite (Fe3O4) nanoparticles-supported dodecylbenzenesulfonic acid (DDBSA@MNP) was synthesized and characterized through different analytical techniques such as TEM, XRD, FTIR, TGA, SEM, EDX and
Green synthesis of trimetallic oxide nanoparticles and their use as an efficient catalyst for the green synthesis of quinoline and spirooxindoles: Antibacterial, cytotoxicity and anti-colon cancer effects
Ali Nasseri, Mohammad,Kazemnejadi, Milad,Keshtkar, Hamideh,Mahmoudi, Boshra,Soleimani, Faezeh
, (2021/09/28)
The three-metallic oxide (Cu/Cr/Ni) nanoparticles were prepared using Echinops persicus plant extract via a simple, biocompatible, cost-effective, and non-toxic procedure, and their catalytic activity was evaluated over the synthesis of biologically activ
An efficient and green microwave-assisted synthesis of quinoline derivatives via knoevengal condensation
Tasqeeruddin, Syed,Asiri, Yahya,Alsherhri, Jaber Abdullah
, p. 157 - 163 (2020/02/04)
We have developed an efficient and green synthesis of quinoline derivatives using L-proline under Knoevenagel condensation. L-proline was found to be an efficient catalyst for the Knoevenagel condensation of substituted 2-aminoaryl ketones 1 with the acti
