The thermodynamic properties of acetals+heptane mixtures at 298.15 K

Excess enthalpies and excess volumes were determined at 298.15 K for: dimethoxymethane+heptane, diethoxymethane+heptane, 1,1-dimethoxyethane+heptane, 1,1-diethoxyethane+heptane, 2,2-dimethoxypropane+heptane and 1,1-diethoxypropane+heptane.     

High-performance liquid radiochromatography: Its application for stability study of [3H] stobadin

An HPLC method was developed for studying the stability of [³H] stobadin stored in physiological saline or buffers at various pH. Optimum conditions for the separation of degradation products were elaborated. A high-performance liquid chromatograph equipped with a radioactivity detector was used.     

Posets isomorphic to their extensions

A standard extension for a poset P is a system Q of lower ends (descending subsets) of P containing all principal ideals of P. An isomorphism between P and Q is called recycling if [Y]Q for all YQ. The existence of such an isomorphism has rather restrictive consequences for the system Q in question. For example, if Q contains all lower ends generated by chains then a recycling isomorphism between P and Q forces Q to be precisely the system of all principal ideals. For certain standard extensions Q, it turns out that every isomorphism between P and Q (if there is any) must be recycling. Our results include the well-known fact that a poset cannot be isomorphic to the system of all lower ends, as well as the fact that a poset is isomorphic to the system of all ideals (i.e., directed lower ends) only if every ideal is principal.     

Stochastic description of a reaction scheme with autocatalysis and saturation law

We apply the master equation and non-linear Fokker-Planck techniques to a model with autocatalysis and (Michaelis-Menten, Langmuir-Hinshelwood) saturation law and the minimal set of reactive steps for a well posed problem is given.     

Additional of functional vinylzinc reagents to nitrones: synthesis of (E)-N-allylhydroxylamines and their rearrangement into (E)-O-allylhydroxylamines

The vinylzinc reagents derived from hydrozirconation of alkynes and transmetallation add readily to nitrones to yield pure (E)-N-allylhydroxylamines; some of these rearrange into O-allylhydroxylamines.     

Syntheses du tri-O-benzyl-3,4,6-D-glucal

The synthesis of 3,4,6 tri-O-benzyl-D-glucal (4) has been accomplished by direct benzylation of triacetylglucal (yield 55%) and by zinc reduction of 3,4,6-tri-O-henzyl-2-acetoxy-1-bromoglucose (yield 26%). The nmr spectra of tribenzyl- and triacetyl-D-glucal in the presence of lanthanide shift reagents were reported.     

Automated multiresidue analysis of pesticides in olive oil by on-line reversed-phase liquid chromatography-gas chromatography using the through oven transfer adsorption-desorption interface

A multiresidue, automated and rapid method for the determination of pesticide residues in olive oil is presented. The method employs the through oven transfer adsorption-desorption interface for the on-line coupling of reversed-phase liquid chromatography and gas chromatography. In this fully automated system, olive oil is directly injected with no sample pre-treatment step other than filtration. Methanol-water is used as eluent in the liquid chromatography pre-separation step. The selected liquid chromatography fraction containing the pesticides is automatically transferred to the gas chromatography. The liquid chromatography column flow during elution is different from the flow during the transfer. Using a flame ionisation detector, pesticide detection limits varied from 0.1 to 0.3 mg/l.