Introduction Over the past 5 years, we have witnessed intense research activity about the
biological potential of natural products (NPs) as human monoamine oxidase B (hMAO-B) …

Cancer continues to be a global health challenge, thereby necessitating the evolution of
innovative therapeutic strategies. The synthesis of chalcone derivatives has garnered …

Chromenes are an essential class of oxygen‐containing heterocyclic compounds with
intriguing biological activity. It is an important moiety for the discovery of new drug …

We present a metal-free strategy to access fluoroalkyl–olefin linkages from fluoroalkane
precursors and vinyl-pinacol boronic ester (BPin) reagents. This reaction sequence is …

In this study, novel selective antitumor compounds were synthesized based on their
fundamental pharmacophoric prerequisites associated with EGFR inhibitors. A molecular …

Herein, we report the synthesis of 2 H-chromenes via catalyst-controlled highly
regioselective [3+ 3] annulation of vinyl sulfoxonium ylides with quinones. Under boron …

Herein, we report a highly efficient Ag (I)-catalyzed indolyzation with Friedel–Crafts
alkylation through a cascade cyclization strategy for accessing valuable hybrid heterocycles …

In order to make the synthesis of pharmaceutically active carbonitriles efficient,
environmentally friendly, and sustainable, the method is regularly examined. Here, we …

Chromenes and 2H‐Chromenes are vital components of natural products, pharmaceuticals,
and agrochemicals that have captured the attention of researchers worldwide. These …

Indole-tethered chromene derivatives were synthesised in a one-pot multicomponent
reaction using N-alkyl-1 H-indole-3-carbaldehydes, 5, 5-dimethylcyclohexane-1, 3-dione …