a highly practical and efficient preparation of pyrano[3,2-c]pyridone and pyrano[3,2-c]quinoline derivatives was developed via an ionic liquid mediated and promoted multi-component reaction of malononitrile, aldehyde, and 4-hydroxyquinolin-2(1h)-one or 4-hydroxy-6-methylpyridin-2(1h)-one. the combinatorial syntheses were achieved for the first time without applying extra activation energy at am...

Quinoline derivatives have been reported to possess multi-therapeutic potential owing the manifestations of different pharmacological effects. The current research work describes about design and synthesis a series novel benzoquinoline analogues with an objective evaluate their antiproliferative structure–activity relationship against colon, breast hepatocellular cancers. Upon synthesis, all de...

Under the catalysis of CuI/2-carboxylic acid-quinoline-N-oxide, the cross coupling reactions between aryl iodides or bromides and aqueous ammonia proceed very well to afford N-unprotected aniline derivatives in excellent yields. This inexpensive catalytic system shows great functional group tolerance and excellent reaction selectivity.

A novel, one-step synthesis of substituted pyridine- and quinoline-derivatives was achieved by acceptorless dehydrogenative coupling of γ-aminoalcohols with secondary alcohols. The reaction involves consecutive C-N and C-C bond formation, catalyzed by a bipyridyl-based ruthenium pincer complex with a base.

Indol-2-ylmethyl carbanions stabilized by alkoxycarbonyl, cyano or benzenesulfonyl groups react with nitroarenes to form σH-adducts, which in the presence of base (triethylamine or DBU) and trimethylchlorosilane transform into indolo[3,2-b]quinoline derivatives in moderate to good yields.

Objective(s): To investigate the efficiency of a novel series of coumarin derivatives bearing benzoheterocycle moiety as novel cholinesterase inhibitors. Materials and Methods: Different 7-hydroxycoumarin derivatives were synthesized via Pechmann or Knoevenagel condensation and conjugated to different benzoheterocycle (8-hydroxyquinoline, 2-mercaptobenzoxazole or 2-mercaptobenzimidazole) using ...

The electrochemical behavior of quinoline in anhydrous liquid ammonia was investigated by cyclic voltammetry and controlled potential coulometry. In the absence of added alkylating agent, quinoline is reduced in two steps to yield the radical anion and dianion both of which undergo further chemical reaction. The radical anion species dimerizes to form the dimeric dianion which is stable in the ...