On the base of 3-formylpicolinic acid by two successive heterocyclizations (the formation of a pyrone fragment by the cyclization of chloroacetone with the carboxyl and formyl groups; and the construction of the thiazole cycle through the bromination of the acetyl fragment and following interaction with thioamides), 6-(2-(phenyl/thiophen-2-yl)thiazole-4-yl)-8H-pyrano[3,4-b]pyridin-8-ones were obtained; and then the pyrone fragment was converted to pyridone by the action of ammonia under high pressure. When such 6-(2-R-thiazol-4-yl)-1,7-naphthyridin-8(7H)-ones reacted with triflic anhydride, O-sulfonylation of the pyridone fragment occurred, after that triflate group was easily substituted by secondary cyclic aliphatic amines. Thus, a number of new 8-amino-6-(2-R-thiazol-4-yl)-1,7-naphthyridines – previously inaccessible heterocyclic derivatives with promising biological activity – were obtained.

The new fully substituted (1H-1,2,3-triazol-4-yl)acetic acids were synthesized from available precursors (1H-1,2,3-triazol-4-yl)ethanones and 1Н-1,2,3-triazole-4-carboxylic acids, which are easily prepared by the Dimroth reaction from azides and 1,3-dicarbonyl compounds. The practical methods of homologization (the Arndt–Eistert reaction and homologization as a result of nucleophilic substitution by cyanide anion) and the Willgerodt-Kindler reaction were compared. The Willgerodt-Kindler method starting from (5-methyl-1H-1,2,3-triazol-4-yl)ethanones was selected as the most convenient method for the synthesis of 2-(1-aryl-5-methyl-1H-1,2,3-triazol-4-yl)acetic acids, which are promising building blocks for drug discovery. Additionally, (1H-1,2,3-triazol-4-yl)ethanones were studied for the synthesis of alcohols, amines and in the Johnson–Corey–Chaykovsky reaction.

A new method of amidation of Carboxy Multi Walled Carbon Nanotubes (MWCNT-COOH) with diamine monomer such as ethylene diamine (EDA) and O-Phenylenediamine (OPDA) was applied by using a solution blending technique. The structure and properties of these composites have been investigated by FTIR, SEM, TEM, XRD, UV, DSC and TGA. The formation of Poly [MWCNT/ Amide] composites was confirmed and the DC electrical conductivity of poly-composites was in the range 4.5×10^-6-5.3×10^-6 S/cm due to the interaction between the nanotubes.

HDPE was functionalized with two different esters in an inert atmosphere at 160°C, under different experimental conditions by thermolysis method. The order of the functionalization and crosslinking reactions was determined. The C=C formation peak is assigned at 1610 cm-1.The percentage of functionalization was determined by FTIR spectroscopy method. Thermogravimetric analysis and differential scanning calorimetric methods were also used to study about the thermal properties of the functionalized HDPE.