The advent of Camptothecin added a new dimension in the field anticancer drug
development containing quinoline motif. Quinoline scaffold plays an important role in …

In the recent past, a number of methods were reported on the application of ultrasound in
organic reactions for the synthesis of diverse organic scaffolds. On the other hand, as far as …

This study reports a nickel-catalyzed sustainable synthesis of polysubstituted quinolines
from α-2-aminoaryl alcohols by a sequential dehydrogenation and condensation process …

An atom-economical and straightforward methodology for the synthesis of quinolines from α-
2-aminoaryl alcohols and secondary alcohols is presented. Using the Earth-abundant and …

The anticancer activities of alkyl esters and NO-donors of ferulic acid (FA) and caffeic acid
(CA) were assessed by a high-throughout screening (HTS) method, and the structure …

A series of novel pyrimido and other fused quinoline derivatives like 4-methyl pyrimido [5, 4-
c] quinoline-2, 5 (1H, 6H)-dione (4a), 4-methyl-2-thioxo-1, 2-dihydropyrimido [5, 4-c] …

A highly efficient I2-catalyzed Povarov-type reaction of methyl ketones, arylamines, and α-
ketoesters is developed. This reaction utilizes a catalytic amount of HI coproduct as a …

A straightforward synthesis of substituted quinolines is described by cyclocondensation of
anilines with 1, 3-diols. The reaction proceeds in mesitylene solution with catalytic amounts …

Copper-Catalyzed Synthesis of Substituted Quinolines via C–N Coupling/Condensation from
ortho-Acylanilines and Alkenyl Iodides | The Journal of Organic Chemistry ACS ACS …

Connexins are a family of transmembrane proteins that are characterized by their capacity to
form intercellular channels called gap junctions that directly link the cytoplasm of adjacent …