The preparation of heterocyclic compounds has attracted great attention in organic
chemistry because of their extensive application in the field of bioactive molecules, materials …

Greener and sustainable synthetic strategies have been evolving as the demanding domain
of organic transformations during the last decade. The division of an environmentally benign …

An efficient synthesis of highly fluorescent trisubstituted thiophenes was achieved via iodine-
catalyzed, base-promoted annulation employing elemental sulfur as a sulfur source. The …

A novel metal-free catalysis protocol for the synthesis of 1, 2-diarylpyrazolo [5, 1-b]
quinazolin-9 (1 H)-ones via intramolecular oxidative C–H amination of (E)-3-(arylamino)-2 …

Two convenient, facile, regioselective and highly effective one-pot protocols for the synthesis
of previously unknown hybrid heterocyclic systems with the furoxanylpyridine core based on …

In this report, we demonstrate that the reaction of nitroarenes with hexamethyldisilane under
various conditions affords a different range of compounds with excellent selectivity. In …

Based on the initial docking studies of a representative compound in silico the evaluation of
SIRT1 inhibitory potential of 2-substituted nicotinic acid ethyl ester derivatives was …

We report here the design and development of a method for the single-step conversion of
esters to ketones with simple reagents. The selective transformation of esters to ketones …

The synthesis and characterisation of six new cationic iridium (III) complexes bearing either
4, 4′-di-tert-butyl-2, 2′-bipyridine (dtBubpy) or 5-NO2-1, 10-phenanthroline along with two …

An environment‐friendly synthetic protocol was developed to access polyfunctionalized
bipyridines from readily available amines, chromone‐3‐carboxaldehydes, and …