A series of novel Ethyl-3-benzoyl-6, 8-difluoroindolizine-1-carboxylate analogues (4a-r)
were synthesized by reacting 3, 5-difluoropyridine, with phenacyl bromide to get quaternary …

A mild, greener approach via tandem-Michael-cyclization cascade reaction towards the
construction of a group of di-and tri-differently substituted indolizine with a broad scope of …

Abstract A series of 1, 2, 3-trisubstituted indolizines (2a–2f, 3a–3d, and 4a–4c) were
screened for in vitro whole-cell anti-tubercular activity against the susceptible H37Rv and …

Candida albicans, an opportunistic fungal pathogen, frequently colonizes immune-
compromised patients and causes mild to severe systemic reactions. Only few antifungal …

An efficient and facile method is developed to synthesize 3-benzoyl indolizines by two-
component reaction under microwave irradiation. A wide range of substrates could be …

This study investigated the phytochemical content of alcoholic extracts and essential oil of a
new variety of medicinal plants, Agastache foeniculum (Pursh), which Kuntze adapted for …

Background: Plant based products are recognised as sources of drugs for treatment of
diseases. Objective: The study aimed at predicting the physicochemical, pharmacokinetics …

A thorough search for the development of innovative drugs to treat tuberculosis, especially
considering the urgent need to address develo** drug resistance, we report here a …

A one-pot three-component method for the synthesis of 3-substituted 2-trifluoromethyl-2, 3-
dihydroimidazo [1, 2-a] pyridin-3-yl analogues from 2-aminopyridine, substituted phenacyl …

Tuberculosis (TB) remains the leading cause of death from an infectious disease globally.
The chemotherapy of TB is complicated by the protracted treatment regimens, development …