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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 300 (1981), S. 143-155 
    ISSN: 1434-601X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We investigate the behaviour of the vacuum charge around a supercritical nucleus withZ〉137 in dependence on the nuclear radius. The screening effects are considered in a quasiclassical approximation. We show that in the point nucleus limit the nuclear charge is screened by the vacuum charge up toZ=137. This means that the coupling strength of a point charge in QED cannot be larger than 1. The influence of the heavier leptons is also discussed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-4475
    Keywords: Acetals ; Desulfurization ; Enantiomerically pure alkanoles ; Thiophenemethanol derivatives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Acetals3 and4 of alkylthienylcarbinols1 were prepared using an enantiomerically pure lactol2. In the key step these compounds were desulfurized. After deprotection the target compounds7 andent-7 were obtained.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 127 (1996), S. 159-165 
    ISSN: 1434-4475
    Keywords: Enantiomerically pure ; Midodrine ; Racemate resolution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary Racemic midodrine chlorohydrate (rac-1) was N-protected to yield the racemic productsrac-2a-c. These were converted into the diastereomeric O-acetals3a-c/4a-c, which can easily be separated by chromatography. After removal of the N- and O-protective groups from3a-b/4a-b, respectively, enantiomerically pure midodrine chlorohydrateR-1 andS-1 could be isolated.
    Notes: Zusammenfassung Das früher präsentierte Verfahren zur Bestimmung der Enantiomerenreinheit von Aminoalkoholen über die N-BOC-O-MBE-Derivate kann auch zur präparativen Trennung von Midodrin eingesetzt werden. Bei Verwendung der N-((Phenylmethoxy)carbonyl)-Schutzgruppe kann die Entfernung der N-Schutzgruppe selektiv vor der Abspaltung der O-MBE-Gruppe erfolgen, so daß die Kontrolle der stereochemischen Einheitlichkeit der Produkte5 und6 sehr leicht möglich ist. Diese können ohne Racemisierung in die enantiomerenreinen MidodrinhydrochlorideR-1 undS-1 übergeführt werden.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1434-4475
    Keywords: 1,2-Amino-alcohols, enantiomerically pure ; Lithium aluminium hydride reduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary A synthesis of β-aminoalcohols is described starting from racemic or enantiomerically pure α-hydroxynitriles which were O-protected using enantiomerically pure acetal type protective groups. Reduction with lithium aluminium hydride yielded O-protected β-aminoalcohols. Whenever diastereomeric O-protected cyanohydrins could not be separated, the mixture was reduced and the resulting O-protected aminoalcohols were separated. Removal of the protective group using hydrogen chloride and methanol yielded enantiomerically pure β-aminoalcohols or their corresponding hydrochlorides.
    Notes: Zusammenfassung Die Reduktion enantiomerenreiner O-MBF- bzw. O-MBE-geschützter Cyanhydrine mit LiAlH4 führt unter Einhaltung definierter Reaktionsbedingungen zu den entsprechenden geschützten Aminoalkoholen, in denen der Anteil der durch Epimerisierung gebildeten Nebenprodukte kleiner als 3% ist. Die Abtrennung der unerwünschten Diastereomere erfolgt im Zuge der Reinigung der Produkte. Durch Schutzgruppenabspaltung mit Salzsäure/Methanol können die enantiomerenreinen Aminoalkohole erhalten werden. Die meist sehr guten Trennfaktoren der O-MBF- bzw. O-MBE-geschützten Verbindungen erlauben für viele Verbindungen sowohl im Cyanhydrin- als auch im Aminoalkoholstadium eine präparative Trennung und machen das Verfahren deshalb vielseitig verwendbar.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1434-4475
    Keywords: 1,2-Amino-alcohols, enantiomerically pure ; N-Alkylation ; Clorprenaline ; Propranolol ; Midodrine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary A synthesis of N-substituted β-aminoalcohols is described starting from enantiomerically pure O-MBF- or O-MBE-protected β-aminoalcohols which can be preparedvia LiAlH4 reduction of O-protected cyanohydrines.
    Notes: Zusammenfassung Clorprenalin und Propranolol können mit dem vorgestellten Verfahren in sehr guter Ausbeute aus den O-MBF-geschützten Aminoalkoholen durch reduktive Alkylierung in enantiomerenreiner Form hergestellt werden. Bei der Synthese von enantiomerenreinem Midodrin, bei der in der letzten Stufe gemeinsam mit der O- auch die N-Schutzgruppe (BOC) abgespalten wird, müssen bestimmte Reaktionsparameter (Zeit, Temperatur) präzise eingehalten werden, um eine entsprechende Enantiomerenreinheit der Endprodukte (〉95% ee) zu gewährleisten.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Planta 149 (1980), S. 341-349 
    ISSN: 1432-2048
    Keywords: Acid phosphatase ; Embryogenesis ; Lytic compartment ; Plastids ; Suspensor ; Phaseolus ; Tropaeolum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Autolysis of the suspensor, an embryonal haustorium, starts in the basal cells and proceeds in the direction of the embryo. InPhaseolus vulgaris, acid phosphatase activity is first found in transforming plastids, similar to the acid phosphatase activity inPh. coccineus [Nagl (1977) Z. Pflanzenphysiol.85, 45–51], although the ultrastructural details are different. InTropaeolum majus, autolysis begins in the most distal part of the suspensor, i.e., the chalazal or carpel haustorium. First the endoplasmic reticulum shows acid phosphatase activity, but neither the mitochondria, which undergo transformation similar to that observed in plastids ofPhaseolus, nor the leucoplasts show such activity. Later, however, the plastids exhibit low activity. Contrarily, the plastids in the suspensor cells adjacent to the embryo show increasing activity during senescence of the suspensor. During final autolysis, activity is found in all cytoplasmic membranes, while it is reduced in plastids. The visible ultrastructural transformations of various organelles into cytolysomes does not necessarily coincide with acid phosphatase activity. Our findings are a further indication of the high diversification and specialization of plastids during plant embryogenesis.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-072X
    Keywords: Methyltransferase ; Membrane protein ; Corrinoids ; Methanogenic bacteria ; Archaebacteria ; Energy conservation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An assay is described that allows the direct measurement of the enzyme activity catalyzing the transfer of the methyl group from N 5-methyltetrahydromethanopterin (CH3−H4MPT) to coenzyme M (H−S−CoM) in methanogenic archaebacteria. With this method the topology, the partial purification, and the catalytic properties of the methyltransferase in methanol- and acetate-grown Methanosarcina barkeri and in H2/CO2-grown Methanobacterium thermoautotrophicum were studied. The enzyme activity was found to be associated almost completely with the membrane fraction and to require detergents for solubilization. The transferase activity in methanol-grown M. barkeri was studied in detail. The membrane fraction exhibited a specific activity of CH3−S−CoM formation from CH3−H4MPT (apparent K m=50 μM) and H−S−CoM (apparent K m=250 μM) of approximately 0.6 μmol·min-1·mg protein-1. For activity the presence of Ti(III) citrate (apparent K m=15 μM) and of ATP (apparent K m=30 μM) were required in catalytic amounts. Ti(III) could be substituted by reduced ferredoxin. ATP could not be substituted by AMP, CTP, GTP, S-adenosylmethionine, or by ATP analogues. The membrane fraction was methylated by CH3−H4MPT in the absence of H−S−CoM. This methylation was dependent on Ti(III) and ATP. The methylated membrane fraction catalyzed the methyltransfer from CH3−H4MPT to H−S−CoM in the absence of ATP and Ti(III). Demethylation in the presence of H−S−CoM also did not require Ti(III) or ATP. Based on these findings a mechanism for the methyltransfer reaction and for the activation of the enzyme is proposed.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 208 (1965), S. 416-422 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary The following method is proposed for the determination of tin in poor tin ores and their dressing wastes: Silicic acid is removed from the raw ore by fuming with hydrofluoric acid, subsequently the sample is fused with sodium peroxide and iron is separated as Fe2O3 · aq by filtration of the alkaline solution of the decomposed material. Any residual iron and other interfering elements are masked by EDTA in ammoniacal medium and tin is precipitated as SnO2 · aq by ammonia in presence of beryllium. The precipitate is dissolved in diluted sulphuric acid and tin is determined as SnIV by colorimetry with phenylfluorone. The method is not liable to systematic errors. Having a confidence level of 95% the variation is ±0.006% (abs.) in the range of 0.0 to at least 0.5% of tin.
    Notes: Zusammenfassung Zur Bestimmung von Zinn in armen Zinnerzen und deren Aufbereitungsabgängen wird folgender Weg vorgeschlagen: Die Kieselsäure des Roherzes wird vor einem Peroxidaufschluß mit Flußsäure abgeraucht und vorliegendes Eisen im wesentlichen als Eisenoxidaquat durch Filtration der alkalischen Aufschlußlösung entfernt. Der Rest des Eisens und alle weiteren Störelemente werden im ammoniakalischen Medium mit ÄDTA maskiert und das Zinn in Gegenwart von Beryllium mit Ammoniak als SnO2 · aq ausgefällt. Der Nederschlag wird in verd. Schwefelsäure aufgelöst und das Zinn als Zinn(IV) mit Phenylfluoron colorimetrisch bestimmt. Das angewandte Analysenverfahren ist frei von systematischen Fehlern und hat bei 95%iger statistischer Sicherheit einen Streubereich von ±0,006% (absolut) im Bereich von 0,0 bis wenigstens 0,5% Zinn.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 139 (1953), S. 188-190 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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