Artificial intelligence in electrostatic risk management

In the last two decades protection against electrostatic hazards became a very important topic. The increase in the range of possible faults fast automated systems and complex fault analysis is required.The tools of artificial intelligence and expert systems have been applied successfully on this field and this paper aims to take a step further. While giving some insight to the currently used tools, another AI method, the 'support vector machines' are introduced in this paper. Besides a brief review on SVMs they are introduced to the SCOUT system, a novel approach to electrostatic hazard management.     

Synthesis and enantiomeric recognition studies of a novel 5,5-dioxophenothiazine-1,9 bis(thiourea) containing glucopyranosyl groups

A novel optically active 5,5-dioxophenothiazine-1,9 bis(thiourea) containing glucopyranosyl groups was synthesized and its enantiomeric recognition properties were examined towards the enantiomers of tetrabutylammonium salts of chiral α-hydroxy and N-protected α-amino acids using UV–vis spectroscopy.     

Addendum to “Ring elements as sums of units”

We give a comment to Theorem 1.1 published in our paper “Ring elements as sums of units” [Cent. Eur. J. Math., 2009, 7(3), 395–399].     

The novel application of Fourier thermal analysis in foundry technologies

The process of casting in sand moulds is used for a large volume of castings manufactured in the world. Internal channels and complex geometries of these products are formed by the placement of cores within the mould cavity. Resin-bound sand mixtures are essential ingredients in engine component manufacturing. In this study, a state-of-the-art application of Fourier thermal analysis in foundry technologies is presented. Investigation of decomposition phenomena of resin-bound moulding materials during casting production is a brand new area to use the potential of thermal sciences. Temperature measurements in test samples of standard types of moulding mixtures were performed. The registered cooling curves were processed by a numerical iteration algorithm to determine the amount of heat absorbed during degradation of the moulding material. Thermogravimetric analysis (TG) and differential thermal analysis (DTA) of sand mixtures were carried out to compare the results of the Fourier thermal analysis with TG and DTA curves.     

Theoretic study of the electronic spectra of neutral and cationic PaO and PaO2

The electronic spectra of neutral PaO and PaO₂ and their mono- (PaO⁺, PaO₂ ⁺) and dications (PaO²⁺, PaO₂ ²⁺) were studied by performing multiconfigurational quantum chemical calculations at the CASSCF/CASPT2 level of theory taking into account spin–orbit coupling. Including the protactinium 7s, 6d, and 5f orbitals as well as selected orbitals of oxygen in the active space, the vertical excitation energies at the ground-state geometries have been computed up to ca. 36,000 cm^?1. The gas-phase electronic spectra at 298 and 3,000 K were evaluated on the basis of the computed oscillator strengths.     

The first synthesis of 3-deoxyoripavine and its utilization in the preparation of 10-deoxyaporphines and cyprodime

The synthesis of 3-deoxyoripavine (7) was realized as a novel and promising intermediate towards the synthesis of the important class of dopaminergic and/or serotonergic 10-deoxyaporphines and the special pharmacological tool µ opioid antagonist cyprodime. Generally, the preparation of these valuable biologically active compounds was achieved in remarkable yields.      

Synthesis of O-α-L-Fucopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-D-glucopyranose. The H-Blood Group Specific Trisaccharide

Abstract

Different reaction conditions were investigated for the preparation of benzyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside (5). Compound 5 on reaction with 2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl bromide afforded the 4-O-substituted 2-acetamido-2-deoxy-β-D-glucopyranosyl derivative which, on O-deacetylation, gave benzyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-4-O-β-D-galactopyranosyl-β-D-glucopyranoside (8). The trimethylsilyl (Me₃Si) derivative of 8, on treatment with pyridineacetic anhydride-acetic acid for 2 days, gave the disaccharide derivative having an O-acetyl group selectively introduced at the primary position and Me₃Si groups at the secondary positions. The latter groups were readily cleaved by treatment with aqueous acetic acid in methanol to afford benzyl 2-acetamido-4-O-(6-O-acetyl-β-D-galactopyranosyl)-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside, which on isopropylidenation gave the desired, key intermediate benzyl 2-acetamido-4-O-(6-O-acetyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside (12). Reaction of 12 with 2,3,4-tri-O-benzyl-α-L-fucopyranosyl bromide under catalysis by bromide ion afforded the trisaccharlde derivative from which the title trisaccharide was obtained by systematic removal of the protective groups. The structures of the final trisaccharide and of various intermediates were established by ¹H and ¹³C NMR spectroscopy.