The new Mannich base VEP (N,N’-bis-(5,5’-diethyl-barbituryl-1-methyl)-piperazine), has been synthetized by condensation of veronal with formaldehyde and piperazine following a Mannich procedure. The new binuclear complex Cu2VEP(X)4·4H2O , X=ClO4where VEP stands for N,N’-bis-(5,5’-diethyl-barbituryl-1-methyl)-piperazine, were obtained by metal ligand direct synthesis. Tetrahedral geometry of the...

Diethyl 2-nitro-(pentafluorosulfanyl)benzylphosphonates, available by the vicarious nucleophilic substitution reaction of meta- and para-nitro-(pentafluorosulfanyl)benzenes and diethyl chloromethylphosphonate, undergo Horner-Wadsworth-Emmons reaction with aldehydes in the presence of potassium hydroxide in acetonitrile at ambient temperature to give (E)-2-nitro-1-alkenyl-(pentafluorosulfanyl)be...

The stereoselective synthesis of diethyl (S)or (R)-IX-[( O-pivaloylhexapyranosyl)amino]benzylphosphonates is achieved via Lewis acid catalyzed addition of diethyl phosphite to O-pivaloylated Nbenzylidene-{3-D-galactosylamine or N-benzylidene-IX-D-arabinopyranosylamine. The process can also be performed by a one-pot procedure selectively giving (S)-aminophosphonic acid derivatives from galactosy...

The title compound, C(29)H(35)N(3), is the product of the condensation reaction between 2,6-diacetyl-pyridine and 2,6-diethyl-aniline. In the mol-ecule, the pyridyl ring is coplanar with the imino functional groups [torsion angles in the range 177.1 (2)-179.9 (2)°. The two 2,6-diethyl-substituted benzene rings are approximately perpendicular to the ethyl-idenepyridine central core, the dihedral...

1,3-Dipolar cycloaddition of the anion of diethyl 1-diazomethylphosphonate, generated in situ from diethyl 1-diazo-2-oxopropylphosphonate (Bestmann-Ohira reagent), with conjugated nitroalkenes provides regioisomerically pure phosphonylpyrazoles in moderate to good yield. These pyrazoles are formed in one pot via spontaneous elimination of the nitro group. However, nitropyrazoles could be synthe...

Effect of temperature on the chemiluminescence (CL) of Luminol in some aqueous aliphatic amines such as ethyl amine (EA), diethyl amine (DEA), and triethyl amine (TEA), have been studied and reported. On the basis of experimental results, it is found that the chemiluminescence intensity initially increased with temperature, attains an optimum value of particular temperature and then decrease on...

Af-Hydroxy-2-acetylaminofluorene was rapidly deacetylated by guinea pig liver and, to a lesser extent, by other guinea pig tissues examined. The enzyme activity was located in the microsomal fraction of the liver. The enzyme appeared to be stimulated by trisodium pentacyanoamine ferrate, and it was inhibited by SKF-525A (|3-diethylaminoethyldiphenylpropyl acetate hydrochloride), by sodium fluor...

The mol-ecule of the title compound, C(17)H(20)N(2)O, a symmetrical derivative of urea, shows non-crystallographic C(2) symmetry. Inter-action with the aromatic system of the phenyl substituents as well as amide-type resonance is responsible for the marked planarization of the coordination environments of the N atoms. C-H⋯O contacts give rise to the formation of centrosymmetric dimers in the cr...

The full mol-ecule of the title compound, C(18)H(18)N(2)O(4), is generated by the application of an inversion centre. There are strong π-π inter-actions between adjacent mol-ecules with a centroid-centroid distance of 3.298 (2)Å.

The serine protease inhibitors diethyl p-nitrophenyl phosphate and phenylmethylsulfonyl fluoride (chemical modifiers of serine residue) and N-acetyl-l-tryptophan ethyl ester (competitive inhibitor of chymotryptic protease) inhibited 1-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine (AGEPC; platelet-activating factor)-induced platelet aggregation and secretion. The inhibition was dependent on the p...