1220115-67-2Relevant articles and documents
Regioselective intramolecular annulations of ambident β-enamino esters: A diversity-oriented synthesis of nitrogen-containing privileged molecules
Yaragorla, Srinivasarao,Pareek, Abhishek
supporting information, p. 909 - 913 (2018/02/12)
Diversity-oriented, regioselective, intramolecular annulation of β-enamino esters is described under solvent-free, calcium-catalysis. 2-aminoaryl ketones and alkyl propiolates undergone a [4+2] annulation to yield substituted quinolines; with an excess of
A simple synthesis of trisubstituted quinolines through transesterification
Patil, Dipti R.,Deshmukh, Madhukar B.,Salunkhe, Sonali M.,Anbhule, Prashant V.
experimental part, p. 1342 - 1346 (2011/12/16)
An efficient and simple method has been reported for the synthesis of 2,3,4-trisubstituted quinolines through zwitterion intermediate under reflux condition in presence of sulfuric acid. The formed dicarboxylate subsequently undergoes transesterification in various alcohols with good yields. Most of the synthesized compounds are newly reported characterized by spectroscopic method. J. Heterocyclic Chem., (2011). Copyright
An improved protocol for the synthesis of quinoline-2,3-dicarboxylates under neutral conditions via biomimetic approach
Madhav, Bandaru,Murthy, Sabbavarapu Narayana,Rao, Kakulapati Rama,Durga Nageswar, Yadavalli Venkata
scheme or table, p. 257 - 260 (2010/05/15)
A mild and efficient protocol for synthesis of quinoline derivatives in aqueous medium under neutral conditions is described. The reaction proceeded smoothly in H2O catalyzed by supramolecular catalyst β-CD. By this protocol, various quinoline derivatives were synthesized in excellent yields.
