The reaction of pyridinium chlorochromate with furan to give enedione derivatives cannot be performed by using commercial PCC. Homemade and commercial PCC had different color and showed some differences in the XRD spectrum. XPS showed the presence of relevant amount of Cr(III) in the homemade reagent. DFT calculations showed that Cr(III) impurities in the reagent can catalyze the reaction with furan derivatives, if oxygen atom in the Cr(III) derivative attacks the furan ring, while it is reoxidized by PCC, through a migration of a chlorine atom.

The corrosion inhibition behavior of cetyl pyridinium chloride (CPC) on mild steel in 0.5 M H2SO4 solution was examined using measurement techniques such as Fourier Transform Infra-red Spectroscopy (FTIR), Field Emission Scanning Electron Microscopy (FESEM), and Atomic Force Microscopy (AFM). The studies were carried out within a 25°C temperature range. The surface morphology of the corroded steel samples was investigated using FESEM and AFM. The results show that cetyl pyridinium chloride (CPC), a mild steel corrosion inhibitor, effectively prevents corrosion in 0.5 M H2SO4 and, when present, increases corrosion resistance. CPC has a stronger inhibitory effect on mild steel. The FESEM and AFM images clearly show how surface morphology changes when additives are present. The weight loss results were confirmed by en-ergy dispersive X-ray (EDX) spectroscopy analysis, and a value of 98.54% was obtained from potentiodynamic polarization studies at 0.0077M CPC. CPC acts as an important corrosion in-hibitor.

A series of N-acyl derivatives of anabasine and cytisine were prepared to discover novel natural product-based medicinal agents. All synthesized compounds were tested for antimicrobial, antifungal, antiviral and analgesic activity. The most pronounced antibacterial activity was shown by the compounds with isoxazole fragments, while adamantane derivatives showed the greatest antiviral effect. It was found that the majority of anabasine derivatives showed significant analgesic activity reducing the pain response of animals to the irritating effect of acetic acid. The presence of a high level of antimicrobial and antiviral activity in newly synthesized compounds makes it possible to consider them promising for further study of their pharmacological properties.