Preparation of novel analgesics via diastereoselective nucleophilic addition to 1-dimethylamino-2-methylpentan-3-one

The diastereoselective synthesis of naphthyl amino alcohols via nucleophilic addition to racemic 1-dimethylamino-2-methylpentan-3-one was studied. The use of the appropriate experimental conditions allowed the synthesis of both diastereoisomers. The relative configurations were established via NOESY experiments.     

Polyelectrolyte complexes. VI. Polycation structure,polyanion molar mass,and polyion concentration effects on complex nanoparticles based on poly(sodium 2‐acrylamido‐2‐methylpropanesulfonate)

The formation and characterization of some interpolyelectrolyte complex (IPEC) nanoparticles based on poly(sodium 2‐acrylamido‐2‐methylpropanesulfonate) (NaPAMPS), as a function of the polycation structure, polyanion molar mass, and polyion concentration, were followed in this work. Poly(diallyldimethylammonium chloride) and two polycations (PCs) containing (N,N‐dimethyl‐2‐hydroxypropyleneammonium chloride) units in the backbone (PCA₅ and PCA₅D₁) were used as starting polyions. The complex stoichiometry, (n^?/n⁺)_iso, was pointed out by optical density at 500 nm (OD₅₀₀), polyelectrolyte titration, and dynamic light scattering. IPEC nanoparticle sizes were influenced by the polycation structure and polyanion molar mass only before the complex stoichiometry, which was higher for the more hydrophilic polycations (PCA₅ and PCA₅D₁) and for a higher NaPAMPS molar mass, and were almost independent of these factors after that, at a flow rate of the added polyion of about 0.28 mL × (mL PC)^?1 × h^?1. The IPEC nanoparticle sizes remained almost constant for more than 2 weeks, both before and after the complex stoichiometry, at low concentrations of polyions. NIPECs as stable colloidal dispersions with positive charges in excess were prepared at a ratio between charges (n^?/n⁺) of 0.7, and their storage colloidal stability, as a function of the polycation structure and polyion concentration (from 0.8 to ca. 7.8 mmol/L), was demonstrated. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2495–2505, 2004     

Tracing Possible Structural Asymmetry of Silica Gel Used for Precoating Thin-Layer Chromatography Plates

JPC – Journal of Planar Chromatography – Modern TLC - We have previously described unexpected two-dimensionality in the thin-layer chromatographic separation of pairs of enantiomers of...     

The Computational Complexity of the Chow Form

We present a bounded probability algorithm for the computation of the Chowforms of the equidimensional components of an algebraic variety. In particular, this gives an alternative procedure for the effective equidimensional decomposition of the variety, since each equidimensional component is characterized by its Chow form. The expected complexity of the algorithm is polynomial in the size and the geometric degree of the input equation system defining the variety. Hence it improves (or meets in some special cases) the complexity of all previous algorithms for computing Chow forms. In addition to this, we clarify the probability and uniformity aspects, which constitutes a further contribution of the paper. The algorithm is based on elimination theory techniques, in line with the geometric resolution algorithm due to M. Giusti, J. Heintz, L. M. Pardo, and their collaborators. In fact, ours can be considered as an extension of their algorithm for zero-dimensional systems to the case of positive-dimensional varieties. The key element for dealing with positive-dimensional varieties is a new Poisson-type product formula. This formula allows us to compute the Chow form of an equidimensional variety from a suitable zero-dimensional fiber. As an application, we obtain an algorithm to compute a subclass of sparse resultants, whose complexity is polynomial in the dimension and the volume of the input set of exponents. As another application, we derive an algorithm for the computation of the (unique) solution of a generic overdetermined polynomial equation system.     

Existence for a degenerate diffusion problem with a nonlinear operator

We study a degenerate nonlinear variational inequality which can be reduced to a multivalued inclusion by an appropriate change of the unknown function. We establish existence, uniqueness and regularity results. An application arising in the theory of water diffusion in porous media is discussed as an example.      

Thermal behaviour of polyacrylamidoxime-copper chelates

The purpose of this work was to investigate the effect of several factors (anion type in the copper salt, pH and concentration of the salt solution) on the structure and thermo-oxidative degradation of the polyacrylamidoxime-copper chelates, by using elemental analysis, IR spectroscopy and dynamic thermogravimetry. The chelates containing copper ions as sulphate exhibit a better initial thermal stability than the polyacrylamidoxime fibre presumably due to the crosslinking generated by the intermolecular complexation of the ions; the removal of the sulphate anions takes place concomitantly with the second step of polymeric chain decomposition. The initial thermal decomposition of the chelates formed by copper ions as nitrate begins at lower temperatures as compared to the polyacrylamidoxime fibre, probably by the nitrate anion release, which partly overlaps the initial decomposition of the copper ion-crosslinked polymeric chains. Copper ions as either sulphate or nitrate catalyse the reactions involved in the main step of polyacrylamidoxime fibre decomposition; the higher the copper amount, the stronger the catalytic effect.     

Group algebras of Kleinian type and groups of units

The algebras of Kleinian type are finite-dimensional semisimple rational algebras A such that the group of units of an order in A is commensurable with a direct product of Kleinian groups. We classify the Schur algebras of Kleinian type and the group algebras of Kleinian type. As an application, we characterize the group rings RG, with R an order in a number field and G a finite group, such that the group of units of RG is virtually a direct product of free-by-free groups.