pyrazine derivatives are important class of compounds with diverse biological and cytotoxic activities and clinical applications. in this study, b3 p 86 / 6 – 31 + + g * was used to compute and map the molecular surface electrostatic potentials of a group of substituted amides of pyrazine-2-carboxylic acids to identify common features related to their subsequent cytotoxicities. several statisti...

Oxidative cyclizations of a variety of heteroatom nucleophiles onto unactivated olefins are catalyzed by palladium(II) and pyridine in the presence of molecular oxygen as the sole stoichiometric oxidant in a nonpolar solvent (toluene). Reactivity studies of a number of N-ligated palladium complexes show that chelating ligands slow the reaction. Nearly identical conditions are applicable to five...

In this study effect of Stearamide as a corrosion inhibitor for mild steel in hydrochloric acid media was investigated employing various electrochemical techniques include potentiodynamic polarization, electrochemical impedance spectroscopy (EIS) and liner polarization resistance (LPR). In view of the fact that Stearamide is an insoluble compound in water, its inhibitive effect was examined by ...

N-Protonation of amides is critical in numerous biological processes, including amide bonds proteolysis and protein folding as well as in organic synthesis as a method to activate amide bonds towards unconventional reactivity. A computational model enabling prediction of protonation at the amide bond nitrogen atom along the C-N rotational pathway is reported. Notably, this study provides a blue...

Chiral 4-[(2-isopropyl-5-methylcyclohexyl)oxo]-4oxobutanoic acid reacts with substituted anilines to produce amides 1-6 in high yields. Resulted amides 1-6 were investigated for their antifungal and antibacterial activities. Compounds 2 (96.5%) against Aspergillus fumigatus and 6 (93.7%) against Helminthosporium sativum demonstrated excellent activities. However, compounds 3 (37.6%) against Bac...

A PCl 3 -mediated conversion of tert-butyl esters into and amides in one-pot under air is developed. This novel protocol highlighted by the synthesis skeletons bioactive molecules gram-scale reactions. Mechanistic studies revealed that this transformation involves formation an acid chloride situ, which followed reactions with alcohols or amines to afford desired products.

Several diand tri-substituted amides of the general formula, 2,6-X2C6H3NHCOCH3−iXi and 2,4,6-X3C6H2NHCOCH3−iXi (X = Cl or CH3 and i = 0, 1, 2, or 3) are prepared, characterised, and their infrared spectra in the solid state and 1H and 13C NMR spectra in solution are studied. The C=O stretching vibrations of N-(2,6-dichlorophenyl)and N-(2,6-dimethylphenyl)-amides appear as strong absorptions in ...

The isolation, crystallization, and partial identification of potato factor II, a stimulator from the chemically neutral fraction of potato extract, is described. The compound was originally found to stimulate elongation of dwarf peas grown under red light, a gibberellin bioassay. It melts between 137 degrees and 139 degrees . In paper chromatography it migrates to R(F) 0.62 in isopropyl alcoho...

A facile, moderate to high yielding synthesis of hexahydro-(di)-benzazocinones is described via an intramolecular N-acyliminium ion cyclisation. The iminium ion intermediates are formed from the readily available 4,4-diethoxybutyl amides with an excess of triflic acid. For electron-withdrawing substituents, better yields were obtained from the pre-formed 2-hydroxypyrrolidine amides. From NMR st...

Fatty acid amide hydrolase (FAAH), also referred to as oleamide hydrolase and anandamide amidohydrolase, is a serine hydrolase responsible for the degradation of endogenous oleamide and anandamide, fatty acid amides that function as chemical messengers. FAAH hydrolyzes a range of fatty acid amides, and the present study examines the relative rates of hydrolysis of a variety of natural and unnat...