The effect of some unsubstituted aromatic amines and their oand p-hydroxylated derivatives on isolated rat-liver mito chondria has been studied. The o-hydroxylated amines inhibited oxygen uptake in the presence of nicotinamide adenine dinucleotide-dependent respiratory substrates. Of the other compounds only l-amino-4-naphthol inhibited oxygen uptake. The Buccinate oxidase system was inhibited ...

A series of interesting sulfonamides containing hydroxyl group were synthesized under solvent-free conditions. The synthetic route involves the selective reaction of amino alcohol and sulfonating agents. The sulfonamides were obtained by simple procedure after an easy work-up in high yield and purity, and characterized by IR, 1H NMR and 13C NMR analysis. These compounds were tested for antibact...

results the dna-dna hybridization experiments between isolate tbz3, h. denitrificans and h. saccharevitans revealed relatedness levels of 57% and 65%, respectively. according to gc-ms results, tbz3 degrades paa to benzene, hexyl butanoate, 3-methyl-1-heptanol and hexyl hexanoate. temperature 32.92°c, ph 6.76, and salinity 14% are the optimum conditions for biodegradation with a confidence level...

2-Amino-substituted ketones react with α-methylene ketones under solvent-free conditions at 90 °C in thepresence of a catalytic amount of zirconium dodecylphosphonate to create the corresponding quinolinesin excellent yields. This procedure recommends numerous advantages such as easy work-up, use of mild,reusable and safe catalyst, short reaction timeand high yields. The new compounds have been...

The present work describes the synthesis of a variety organotellurium compounds. first part new series compounds containing azomethine groups. Reaction (E)-(4-((1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ylidene)amino)phenyl)mercury(II)chloride and (E)-(5-methyl-2-((1,7,7-trimethylbicyclo[2.2.1]heptan-2-ylidene)amino)phenyl) mercury(II)chloride with tellurium tetrabromide in 2:1 mole ratio yielded ...

Tetrahydrofuran aminolignans bearing an amino group at the 8 position were synthesized via an N,O-heterocyclic compound that had been obtained by silylnitronate cycloaddition.

A three-step procedure for the synthesis of multifunctionalized heterocycles from a pyroglutamic acid derivative, glycidyl components and anilines by nucleophilic substitution and cobalt catalysis is presented.

The structural motif of α,α-difluoro-substituted carboxyl and carbonyl groups with hydroxy- or amino-substituents at the stereogenic carbon in β-position is found frequently drugs biologically active compounds. A straightforward method for obtaining those targets high enantiomeric purity given by asymmetric difluoro-Reformatsky imino-difluoro-Reformatsky reactions that lead to α,α-difluorinated...

The synthesis of new derivatives 2-[(1,4-dioxo-1-amino-4-arylbutyl-2-en-2-yl)amino]-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid is described. Starting 2-{[5-aryl-2-oxofuran-3(2H)-ylidene]amino}thiophene-3-carboxylic acids were obtained by intramolecular cyclisation substituted 4-aryl-4-oxo-2-thienylaminobut-2-enoic in acetic anhydride. New via decyclization reaction acids. structure t...