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Exploring the redox mechanism of 9-acridinyl amino acid derivatives by electrochemical and theoretical approach
Acridine analogues represent a diverse class of compounds known for their broad spectrum of biological activities, including anticancer, antibacterial, antiviral, antimalarial, antiparasitic, and fungicidal effects [1]. Their biological activity is largely attributed to the planar heterocyclic structure of the polyaromatic core, which facilitates intercalation between double-stranded DNA (dsDNA) base pairs, thereby affecting vital cellular processes [2].
Vibrational assignments, normal coordinates analysis, force constants, and DFT/MP2 computations of 5-Chloro-2,4,6-trifluoropyrimidine
The heterocyclic aromatic six-membered pyrimidine has two nitrogen atoms in positions 1 and 3, with two more diazine forms and isomers.
Utilization of ruthenium(0) for σ-bond activation: Formation of organoruthenium complexes and emergence of their catalytic activity via in situ Ru-C bond cleavage
In this paper we report the successful utilization of ruthenium(0) for phenolic O H followed by aryl C H bond activations leading to the formation of ruthenium-hydrido and cycloruthenated complexes; and catalytic efficiency of these complexes towards transfer-hydrogenation (TH) of selected substrates.
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