A PASE-based approach towards 12-(1H-1,2,3-triazol-1-yl)-indolo[2,1-a]isoquinolines via the reaction of 3-(isoquinolin-1-yl)-1,2,4-triazines with benzyne

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Optimal Kα XRF detection geometry of arsenic in skin using an extended fundamental parameter method

The fundamental parameter (FP) method was extended to account for the geometrical details of experimental x‐ray fluorescence (XRF) detection. In the traditional FP method the primary fluorescence photons have parallel pathways towards the detector. In the new approach the primary fluorescence photons can travel in any direction which allows them to reach the detector if not absorbed or scattered. The derived XRF signal equation explicitly depends on the length of the collimator in front of the detector, the detector size, position and orientation. An algorithm which numerically calculates the XRF signal for any set of parameters was developed and implemented for the K_α XRF signal of arsenic in skin. Optimal positions and orientations of the detector and collimator ensemble which maximize the XRF signal were found. Results and limitations of the method were also discussed. Copyright © 2009 John Wiley & Sons, Ltd.     

Determination of resveratrol and piceid in beer matrices by solid-phase extraction and liquid chromatography-tandem mass spectrometry

Beer is one of the most commonly consumed undistilled alcoholic beverages in many countries. In recent studies, the stilbenes resveratrol and piceid have been found in some hop varieties which are used in the production of beer. Therefore, they could be transferred to beer. The aim of the present work was to validate a method to study the potential content of trans- and cis-resveratrol and piceid in 110 commercial beers from around the world. The resveratrol and piceid contents of 110 beers were analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) after a solid-phase extraction (SPE) using optimized and validated procedures for the beer matrix. The beer matrix effect was also studied. Stilbenes were found in quantifiable amounts in 92 beers, while concentrations below the limit of quantification (LOQ) were found in 18 beers. Resveratrol was found in the range of 1.34-77.0μg/L in 79% of the beers analyzed, and piceid was found in the range of 1.80-27.3μg/L in only 33% of them. The mean of total resveratrol in all the beers was 14.7±20.5μg/L. The content of resveratrol has been compared with other resveratrol containing foods. A serving of beer contains similar amounts of stilbenes as berries, less than chocolate and grape products but more than pistachios, peanuts or tomatoes. Overall, beer is one of the products with the lowest levels of total resveratrol (μg/L), and despite its high consumption it should not be considered as a representative source of resveratrol.     

Corticomuscular synchronization with small and large dynamic force output

Background  

Over the last few years much research has been devoted to investigating the synchronization between cortical motor and muscular activity as measured by EEG/MEG-EMG coherence. The main focus so far has been on corticomuscular coherence (CMC) during static force condition, for which coherence in beta-range has been described. In contrast, we showed in a recent study [1] that dynamic force condition is accompanied by gamma-range CMC. The modulation of the CMC by various dynamic force amplitudes, however, remained uninvestigated. The present study addresses this question. We examined eight healthy human subjects. EEG and surface EMG were recorded simultaneously. The visuomotor task consisted in isometric compensation for 3 forces (static, small and large dynamic) generated by a manipulandum. The CMC, the cortical EEG spectral power (SP), the EMG SP and the errors in motor performance (as the difference between target and exerted force) were analyzed.     

Reaction of Frustrated Lewis Pairs with Ketones and Esters

The frustrated Lewis pair (FLP) Mes₂PCH₂CH₂B(C₆F₅)₂ ( 1 ) reacts with an enolizable conjugated ynone by 1,4‐addition involving enolate tautomerization to give an eight‐membered zwitterionic heterocycle. The conjugated endione PhCO‐CH?CH‐COPh reacts with the intermolecular FLP tBu₃P/B(C₆F₅)₃ by a simple 1,4‐addition to an enone subunit. The same substrate undergoes a more complex reaction with the FLP 1 that involves internal acetal formation to give a heterobicyclic zwitterionic product. FLP 1 reacts with dimethyl maleate by selective overall addition to the C?C double bond to give a six‐membered heterocycle. It adds analogously to the triple bond of an acetylenic ester to give a similarly structured six‐membered heterocycle. The intermolecular FLP P(o‐tolyl)₃/B(C₆F₅)₃ reacts analogously with acetylenic ester by trans‐addition to the carbon–carbon triple bond. An excess of the intermolecular FLP tBu₃P/B(C₆F₅)₃, which contains a more nucleophilic phosphane, reacts differently with acetylenic ester examples, namely by O? C(alkyl) bond cleavage to give the {R‐CO₂[B(C₆F₅)₃]₂^?}[alkyl‐PtBu₃⁺] salts. Simple aryl or alkyl esters react analogously by using the borane‐stabilized carboxylates as good leaving groups. All essential products were characterized by X‐ray diffraction.     

Dirac’s Theorem on Simplicial Matroids

We introduce the notion of k-hyperclique complexes, i.e., the largest simplicial complexes on the set [n] with a fixed k-skeleton. These simplicial complexes are a higher-dimensional analogue of clique (or flag) complexes (case k = 2) and they are a rich new class of simplicial complexes. We show that Dirac’s theorem on chordal graphs has a higher-dimensional analogue in which graphs and clique complexes get replaced, respectively, by simplicial matroids and k-hyperclique complexes. We prove also a higher-dimensional analogue of Stanley’s reformulation of Dirac’s theorem on chordal graphs.      

Disintegration-of-measure techniques for commuting multivariable weighted shifts

We employ techniques from the theory of disintegration of measuresto study the Lifting Problem for commuting n-tuples of subnormalweighted shifts. We obtain a new necessary condition for theexistence of a lifting, and generate new pathology associatedwith bringing together the Berger measures associated to eachindividual weighted shift. For subnormal 2-variable weightedshifts, we then find the precise relation between the Bergermeasure of the pair and the Berger measures of the shifts associatedto horizontal rows and vertical columns of weights. 2000 MathematicsSubject Classification 47B20, 47B37, 47A13, 28A50 (primary),44A60, 47-04, 47A20 (secondary).     

Complementary aspects of diffusion imaging and fMRI; I: structure and function

Studying the intersection of brain structure and function is an important aspect of modern neuroscience. The development of magnetic resonance imaging (MRI) over the last 25 years has provided new and powerful tools for the study of brain structure and function. Two tools in particular, diffusion imaging and functional MRI (fMRI), are playing increasingly important roles in elucidating the complementary aspects of brain structure and function. In this work, we review basic technical features of diffusion imaging and fMRI for studying the integrity of white matter structural components and for determining the location and extent of cortical activation in gray matter, respectively. We then review a growing body of literature in which the complementary aspects of diffusion imaging and fMRI, applied as separate examinations but analyzed in tandem, have been exploited to enhance our knowledge of brain structure and function.