Pyrimidine compounds continue to attract great interest in the field of organic synthesis due to their various chemical and biological applications observed, especially in recent times. As a result, this review covering some periods from 1957 to 2021 has been prepared to discuss some of the structural pathways of these compounds as well as some of their interactions and applications.

A new series of 2-[3-(5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)-1-phenyl-1H-4-pyrazolyl]-3-aryl-1,3-thiazolan-4-one 5(a-i) have been designed, synthesized and evaluated for their in vitro antibacterial activity against Gram positive bacteria viz. Bacillus subtilis (ATCC 6633), Staphylococcus aureus (ATCC 6538p), Micrococcus luteus (IFC 12708) and Gram negative bacteria viz. Proteus vulgaris (ATCC 3851), Salmonella typhimurium (ATCC 14028), Escherichia coli (ATCC 25922) the antifungal activity against Candida albicans (ATCC 10231), Aspergillus fumigatus (HIC 6094), Trichophyton rubrum (IFO 9185), Trichophyton mentagrophytes (IFO 40996). Antibacterial evaluation indicates that compounds containing 4-methoxyphenyl 5c, 4-fluorophenyl 5d and 2,5-difluorophenyl 5h groups on thiazolidinone ring showed significant activity equal to that of standard drug. The antifungal evaluation shows that compound 5c is highly active against A. fumigatus, compound 5d and 5h were also active against C. albicans and A. fumigatus.

Different methods for the synthesis of pyridine derivatives as well as the chemical reactivity profiles and structures of these substances are reviewed. The utility of these compounds as precursors is emphasized in the synthesis of many heterocycles that are pharmacologically active organic compounds and agrochemicals. This review results from a literature survey containing some synthetic methods and applications of pyridine derivatives.

Reaction of N-cyanoguanidine with acid chlorides and aroylisothiocyanates gave the respective; N-(N-cyanocarbamimidoyl)aryl-2-carboxamides 1-5 and N-[(N-cyanocarbamimidoyl)carbamothioyl]benzamides 6-10, which have a Neonictinoid insecticide’s active group moiety (=N–CN). They have more toxicological activity against wheat Aphid (Schizaphis graminum) than Spodoptera littoralis.

Due to the complicated problems coming from excessive applications of insecticides, searching for safe substitutes to these insecticides has become a necessity. Thus, the insect growth regulators are candidates to be used in such concern. Comparative studies of the effects of three compounds, 2-benzoyl-N-phenylhydrazine-1-carbothioamide (1), 2-(cyanoacetyl)-N-phenylhydrazine-1-carboxamide (2) and N-(2-(2-cyanoacetyl)hydrazinecarbonothioyl)furan-2-carboxamide (3) (an insect growth regulator inhibiting chitin synthesis), were conducted on Spodoptera littoralis (Boisduval, 1833). The compounds, orally administered, caused larval mortality proportional to the concentrations in the food source. larvae were unable to complete the molting process and died in the old larval cuticle. Larvae contaminated by sublethal doses completed their development to adulthood. N-(2-(2-cyanoacetyl)hydrazinecarbonothioyl)furan-2-carboxamide (3) is more active than the other compounds have LC50 17.082 ppm for 2nd instar larvae and 60.832 ppm for 4th instar larvae.

In this review we systematized the theoretical and experimental data concerning the versatile approaches for the synthesis of N-acylphenothiazines. The aim of the study was to compile the literature reported worldwide in the past 20 years. This article also reviewed the analysis of pharmacological activities of these heterocycles as one of the promising chemotherapeutic objects for the modern bioorganic and medicinal chemistry. It has been hypothesized that the enormous biological potential of these moieties is due to the radical nature in the acyl moiety. Therefore, the present review will be a good contribution to the literature and will provide the platform for the medicinal chemistry researchers to carry out more studies aiming the N-acylphenothiazine moieties as the novel chemotherapeutic agents.

Biologically active organic compounds continue to attract great interest due to the wide variety of interesting applications observed for these compounds. This review results from the literature survey containing the organic compounds that are used as insect growth regulators with a focus on their mode of action and some synthetic routes.

Regioselective acylation of monosaccharides are highly significant for the preparation of both natural and non-natural carbohydrate compounds and their synthetic intermediates. In this respect, an efficient simple method for site selective 6-O-hexanoylation of octyl β-D-glucopyranoside (OG) at low temperature is described. The 6-O-hexanoylglucoside, thus formed, was then treated with five acyl halides and obtained novel corresponding O-acylglupyranosides at C-2, C-3 and C-4 positions with high yields. Activity spectra prediction for substances (PASS) indicated that these glucoside esters are potential against antimicrobials especially against fungi. In vitro antibacterial test indicated them as weak to moderate inhibitor of Gram-positive organisms. ADMET prediction indicated that these OGs are overall safe to use. Density functional theory (DFT) optimized electronic energy, enthalpy (ΔH), Gibbs free energy, entropy, dipole-moment (μ), and molecular electrostatic potential (MEP) are also discussed.

Amidoalkylation of secondary heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]-2'-chloroacetamide resulted the new compounds 5-10 that contain 1,3,4-thiadiazole-5-thione moiety alongside pyperidine, morpholine, and cytisine fragments. In vitro screening of antimicrobial activity of synthesized compounds showed that N-[5-(amylsulfanyl)-1,3,4-thiadiazol-2-yl]-2'-morpholinacetamide exhibited an appreciable antibacterial activity against gram-negative bacteria of Escherichia coli (inhibition zone diameter of 16 mm) and gram-positive bacteria of Staphylococcus aureus and Bacillus subtilis (10-13 mm).

The aim of the research was to analyse fragrance allergens in selected alcohol-based perfumery products with the application of gas chromatography. Toilet waters and scented waters were analysed. Samples of the selected perfumery products were tested for the presence of typical allergens, such as linalool, citral, citronellol, geraniol, eugenol and alpha-isomethyl ionone, in the so-called fragrance concentrate. The obtained results showed that each of the products contained at least a few of the above-mentioned allergens. Nevertheless, the majority of the analysed products satisfied the recommendations of the Scientific Committee on Cosmetic Products and Non-food Products valid for cosmetics intended to remain on the skin for some time.