A C-glycoside route to leukotrienes

The stereospecific syntheses of three isomers of 7-hydroxy-5,6-epoxy heptanoic acid methyl ester, $\text{7}$, $\text{12b}$ and $\text{19}$, have been achieved via a $\text{C}$-glycoside route.     

Preparation of ethyl 5(s),6-epoxy-3(r)-(methoxymethoxy)hexanoate: a key chiral intermediate for mevinolin and compactin.

The synthesis of Ethyl 5(S),6-Epoxy-3(R)-(methoxymethoxy)hexanoate, a key chiral synthon for the β-hydroxy-δ-lactone portion of Mevinolin and Compactin, $\text{via}$ a regiospecific ring opening of a tetrahydrofuran derivative by dimethylboron bromide, is described.     

Synthesis and stereochemistry of some new 1,3,5-tris(1,3-dioxan-2-yl)-benzene derivatives

The synthesis and the stereochemistry of new 1,3,5-tris(1,3-dioxan-2-yl)-benzene derivatives are reported. The anancomeric structure and the axial orientation of the aryl group with respect to all 1,3-dioxane rings, and the cis-trans isomerism of some of the compounds are revealed. The data are supported by NMR investigations and by the molecular structure of one compound determined by single crystal X-ray diffractometry.     

On the convergence rate of the conjugate gradients in presence of rounding errors

Summary We investigate here rounding error effects on the convergence rate of the conjugate gradients. More precisely, we analyse on both theoretical and experimental basis how finite precision arithmetic affects known bounds on iteration numbers when the spectrum of the system matrix presents small or large isolated eigenvalues.The present work was supported by the Programme d'impulsion en Technologie l'Information, financed by Belgian State, under contract No. IT/IF/14Supported by the Fonds National de la Recherche Scientifique, Chargé de recherches     

The dielectric function of LnSF rare-earth fluorosulfides (Ln=La, Ce): experiment and theory

The absorption properties of LaSF and CeSF in the UV-Visible range have been investigated on the basis of first principles density functional theory (DFT) calculations and from electron energy-loss spectroscopy (EELS) measurements. The extinction coefficient k, as well as the refractive index n, determined experimentally from the loss function Im(−1/ε), were compared with the corresponding factors extracted from the calculated dielectric tensor ε₂. The k and n values for the two compounds were expected to be very close to each other, owing to the chemical similarity of La and Ce. However, it was found that the nature of the electronic transitions in LaSF and CeSF strongly influences the k and n values with the result that the refractive index n and the extinction coefficient k are substantially larger for LaSF than for CeSF.     

Coupled structural and magnetic properties of ferric fluoride nanostructures: Part II,a Monte Carlo–Heisenberg study

We present a numerical study of the magnetic structure of nanostructured iron fluoride, using the Monte Carlo Metropolis simulated annealing technique and a classical Heisenberg Hamiltonian with superexchange angle dependent interactions. The parameters are adjusted on experimental results, and the atomic structure and topology taken from a previous atomistic model of grain boundaries in the same system. We find perfect antiferromagnetic crystalline grains and a disordered magnetic configuration (speromagnetic) at the grain boundary, in agreement with experimental features. Both the lowest magnetic energy and the rate of magnetic frustration are found to be dependent on the relative disorientation of crystalline grains, i.e. on the cationic topology. We conclude on possible extensions of the model.     

Pressure‐assisted CEC versus CEC using methacrylate‐based monolithic columns: Influence of the polymerization‐mixture composition

Pressure‐assisted CEC (pCEC) can either be performed on a CE instrument by adding pressure at the column inlet, or by applying voltage on a capillary liquid chromatography system. This study investigates the pressure's added value in pCEC using an LC instrument as well as the influence of the polymerization‐mixture composition on monolithic columns in such experimental circumstances. Two factors of the polymerization mixture, which is used to prepare the monolithic capillary columns, were varied according to an experimental design approach: the pore‐forming solvent/total monomer ratio and the pore‐forming solvents composition. Initially, the effect of the resulting stationary phase on the elution behavior of mainly pharmaceutical compounds was studied. Four responses were used to evaluate the effects on the chromatography: retention time, retention factor, peak asymmetry and number of theoretical plates. After processing the results, the stationary phase composition with the best chromatographic behavior was determined and tested. The advantageous properties of this stationary phase compared with the design center‐point column were demonstrated. Secondly, the results of these pCEC experiments were compared with those generated in an identical experimental setup previously performed using CEC. Chromatographic conditions were chosen so that the center‐point column showed similar retention in CEC and pCEC. The expected advantage (faster analysis) and drawback (decreased efficiency) of pCEC in the analysis of pharmaceuticals was evaluated. Analysis time and efficiency were both found to depend greatly on the porosity of the column. The conclusion of this comparison is that pCEC did not have a significant added value to CEC. However, this was mainly due to the instrument's limitation of the pressure‐driven flow over the column. A clear benefit of the pCEC setup was apparatus‐related, i.e. the presence of a loop injection system on the pCEC instrument, which avoids the injection problems that were occasionally observed in CEC.