128832-35-9Relevant 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
Novel Acyl-CoA:Cholesterol Acyltransferase Inhibitors. Synthesis and Biological Activity of 3-Quinolylurea Derivatives
Tawada, Hiroyuki,Harcourt, Myles,Kawamura, Noriaki,Kajino, Masahiro,Ishikawa, Eiichiro,et al.
, p. 2079 - 2084 (2007/10/02)
A series of 3-quinolylurea derivatives (1) was synthesized and evaluated for acyl-CoA:cholesterol acyltransferase (ACAT) inhibitory activity.For in vitro studies, the most potent inhibitory activity was found in derivatives having substituents at the 6,7-