The synthesis of y-glutamylhydroxamic acid from glutamine and hydroxylamine is catalyzed by glutamine synthetase in the presence of adenosine diphosphate, inorganic phosphate, and magnesium ions (l), and also by other enzyme preparations (2,3) that do not exhibit a requirement for nucleotides or metal ions. The synthesis of y-glutamylhydroxamic acid from glutamic acid and hydroxylamine that is ...

In the title mol-ecular salt, C12H12N2 (2+)·2C7H5O5S(-), the complete dication is generated by crystallographic inversion symmetry. In the anion, the sulfonic acid group is deprotonated and the dihedral angle between the planes of the carb-oxy-lic acid group and the benzene ring is 12.41 (11)°. In the crystal, the anions are linked into inversion dimers by pairs of O-H⋯O hydrogen bonds, which g...

The synthesis of y-glutamylhydroxamic acid from glutamine and hydroxylamine is catalyzed by glutamine synthetase in the presence of adenosine diphosphate, inorganic phosphate, and magnesium ions (l), and also by other enzyme preparations (2,3) that do not exhibit a requirement for nucleotides or metal ions. The synthesis of y-glutamylhydroxamic acid from glutamic acid and hydroxylamine that is ...

The current work utilizes the ab initio density functional theory (DFT) to develop a molecular level of the mechanistic understanding on the phenol alkylation in the presence of a cation-exchange resin catalyst, Amberlyst-15. The catalyst is modeled with the benzene sulfonic acid, and the effect of this acid on olefins such as isopropene (i-Pr) and tributene (t-Bu) in a phenol solution mimics t...

3-methyl-1-sulfonic acid imidazolium tetrachloroferrate {[Msim]FeCl4} as an efficient sulfur catalyst was prepared and applied, as an efficient catalyst, for the cross-aldol condensation reaction between cycloalkanones and arylaldehydes to give α,αʹ- bis(arylidene)cycloalkanones in high yields and short reaction times at 75 °C under solvent-free conditions. 3-methyl-1-sulfonic acid imidazolium...

The title compound, C(18)H(12)N(6)O(6), was prepared from the reaction of 4-(phenyl-diazen-yl)aniline (aniline yellow) with picryl-sulfonic acid. The dihedral angle formed by the two benzene rings of the diphenyl-diazenyl ring system is 6.55 (13)° and that formed by the rings of the picrate-aniline ring system is 48.76 (12)°. The mol-ecule contains an intra-molecular aniline-nitro N-H⋯O hydroge...

A novel rhodium-catalyzed imination of sulfoxides using O-(2,4-dinitrophenyl)hydroxylamine is developed under mild conditions with good functional group tolerance. This method provides an efficient access to free NH-sulfoximines, an important structural unit in a variety of biologically active compounds.