In multicomponent reactions, three or more reactants combine in one pot to form a product
without the isolation of intermediate and most of the reactants contribute to newly formed …

Pyrroles and their fused compounds are widely known as biologically active scaffolds, which
are mainly fused at the 1–2 (a), 2–3 (b), 3–4 (c) and 4–5 (d) positions. In pyrrole ring …

Herein, we report an efficient methodology for the synthesis of alkyl, benzyl, and phenyl
selenoethers of aminopyrazoles and aminouracils by C (sp2)–H functionalization in the …

Herein, we report a metal-free one-pot three-component reaction of aryl methyl ketones, 2-
aminopyridines, and barbituric acids for the synthesis of pyrimidine-linked imidazopyridines …

Herein we report a metal-free multicomponent reaction for the synthesis of diverse quinoline-
fused pyrroles using 1, 1, 1, 3, 3, 3-hexafluoro isopropanol (HFIP) as a reaction medium cum …

The widespread scrutiny of orthodox synthetic techniques for the fabrication of nitrogen-
embracing heteroatom segments has shifted scholar's focus to innovative environmentally …

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

A straightforward and effective method for synthesizing coumarin-linked pyrrole derivatives
fused with naphthoquinone has been reported by the one-pot reaction of aryl glyoxal, 4 …

Pyrrole is an essential chemical with considerable relevance as a pharmaceutical
framework for many biologically necessary medications. The growing demand for …

Alkynes have two active positions to carry out chemical reactions: CC and C–H. These two
positions are involved and activated in different reactions using different reagents. In this …