116690-74-5Relevant articles and documents
PEG-SO3H as a catalyst in aqueous media: A simple, proficient and green approach for the synthesis of quinoline derivatives
Nasseri,Alavi,Zakerinasab
, p. 109 - 116 (2013)
A convenient and efficient method was developed for the synthesis of quinolines, an important class of potentially bioactive compounds. The quinoline derivatives were prepared in water, an excellent solvent in terms of environmental impact and with reduce
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
A simple, efficient and solvent-free protocol for the friedlaender synthesis of quinolines by using SnCl2·2H2O
Arumugam, Pandurangan,Karthikeyan, Ganesan,Atchudan, Raji,Muralidharan,Perumal, Paramasivan T.
, p. 314 - 315 (2007/10/03)
A variety of polysubstituted quinolines have been synthesized under solvent free condition by using tin(II) chloride-dihydrate. The reaction proceeds smoothly at room temperature in short reaction time. The yields and purity are excellent. Copyright
The Preparation of Quinolines and Related Fused-Ring Heterocycles from the Dianions of Benzoylacetone, Certain Cyclic Ketone Oximes, or Certain Substituted Hydrazones
Mack, H. Michael,Davis, Everette A.,Kadkhodayan, Babak,Taylor, Richard A.,Duncan, Dean C.,Beam, Charles F.
, p. 1733 - 1740 (2007/10/02)
C(α),O-Dilithiooximes, C(α),N-dilithiobenzoylhydrazones, or C(α),N-dilithiocarboalkoxyhydrazones were prepared in an excess of lithium diisopropylamide (LDA) and condensed with 2-aminobenzophenones, or isatoic anhydrides to give intermediates that were treated with aqueous acid, which caused their hydrolysis, cyclodehydration and/or linear dehydration to give products which were substituted quinolines or related fused-ring heterocycles (e.g., cycloheptaquinolines).Dilithiobenzoylacetone was condensed with 2-aminobenzophenones, which was followed by acid cyclodehydration to substituted 2-phenacylquinolines.
