The interest in synthesizing heterocycles has always been enormous. The literature contains
a variety of synthetic approaches to the heterocycle ring structures, much of which has been …

Quinoline or 1-aza-naphthalene is a weak tertiary base. Quinoline ring has been found to
possess antimalarial, anti-bacterial, antifungal, anthelmintic, cardiotonic, anticonvulsant, anti …

Although three new drugs or drug formulations, liposomal amphotericin B (AmBisome),
miltefosine and paromomycin should be available for the treatment of visceral leishmaniasis …

A novel, one-step synthesis of substituted pyridine-and quinoline-derivatives was achieved
by acceptorless dehydrogenative coupling of γ-aminoalcohols with secondary alcohols. The …

A series of 29 new quinoxalines was synthesized and evaluated in vitro against several
parasites (Leishmania donovani, Trypanosoma brucei brucei, and Trichomonas vaginalis) …

We report herein the synthesis and biological activities (cytotoxicity, leishmanicidal and
trypanocidal) of six quinoline-chalcone and five quinoline-chromone hybrids. The …

Quinolines are a prominent heterocyclic motif and crucial building blocks in creating
physiologically active compounds. Due to the fast development of novel medicines with a …

Herein we describe our results on the synthesis and antioxidant properties of 4-
arylchalcogenyl-7-chloroquinolines. This new class of compounds has been synthesized in …

A highly efficient synthesis of trans-alkenylazaarene under catalyst-free conditions was
developed via the addition of methylazaarenes to N-sulfonyl aldimines and a subsequent C …

An efficient one pot synthesis of a series of pluripotent (E)-1-(3-methyl-5-aryl-7-styryl-5H-
thiazolo [3, 2-a] pyrimidin-6-yl)-3-arylprop-2-en-1-ones is reported. It involves reaction of 5 …