Cancer is one of the most fatal threatens to human health throughout the world. The major
challenges in the control and eradication of cancers are the continuous emergency of drug …

The emergence and worldwide spread of drug‐resistant bacteria have already posed a
serious threat to human life, creating the urgent need to develop potent and novel …

Organometallic compounds have gained popularity as potent anti-cancer therapeutic
prospects in recent years. The constant threat of drug-resistant cancer and the limited …

Functionalization of ferrocenyl hydrazone with rhodamine based tag using solid state
synthetic method led to the formation of molecules containing both, fluorescent active and …

Unsymmetrically bi-functionalized ferrocenyl compounds are significant class of
multifunctional molecule having unique structural features, varied conformational …

Destabilization of protein's native conformation to intermediates rich in β-sheet structure may
lead to amyloid fibrillation involving a complex process of aggregation that are primarily …

Selective funtionalization of ferrocenyl species with fluorescent active rhodamine moiety
using a solvent free solid state method led to the synthesis of 1, 1'-unsymmetrical ferrocene …

Imidazolidinone derivatives have emerged as promising anticancer agents, captivating the
attention of researchers in medicinal chemistry. Imidazolidinones, characterized by their …

Facile synthesis of cyanovinylhydrazone bridged diferrocenyl compounds using a unique
solid state synthetic method led to the formation of donor-acceptor type compounds with …

Abstract A series of 1, 1′-unsymmetrical bi-functionalized ferrocenyl hydrazone–enone
molecular compounds (3–7) have been synthesized using a facile redmud supported solid …