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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 2695-2698 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Easy Syntheses of Sulfur-Nitrogen CompoundsThe sulfonamide CF3SO2NH2 (2a) reacts with S3N2Cl2 1, which can be prepared from urea and S2Cl2, to yield S3N3SO2CF3 3 with formation of hydrogen chloride while CH3SO2NH2 (2b) yields (CH3SO2NSN)2S 4 under cleavage of the ring system of 1. Under similar conditions 1 reacts with SO2(NH2)2 to form S4N4O2 5. The structure of 5 is confirmed by X-ray analysis. The hydrolysis of 1 with anhydrous formic acid or acetic anhydride yields S3N2O 6. Five-membered S3N2-rings 9a-c are formed by the reaction of S4N4 with the anhydrides (FSO2)2O, (CF3CO)2O, and (CCl3CO)2O.
    Notes: Das Sulfonsäureamid CF3SO2NH2 (2a) reagiert mit S3N2Cl2 1, das aus Harnstoff und S2Cl2 hergestellt werden kann, unter Chlorwasserstoffabspaltung zu S3N3SO2CF3 3, während CH3SO2NH2 (2 b) unter Ringspaltung (CH3SO2NSN)2S 4 bildet. 1 und SO2(NH2)2 ergeben unter ähnlichen Bedingungen S4N4O2 5, dessen Struktur durch Röntgenstrukturanalyse bestätigt wird. Die Hydrolyse von 1 liefert mit wasserfreier Ameisensäure oder Acetanhydrid S3N2O 6. Fünfgliedrige S3N2-Ringe 9a-c lassen sich auch darstellen, wenn S4N4 mit den Anhydriden (FSO2)2O, (CF3CO)2O und (CCl3CO)2O umgesetzt wird.
    Additional Material: 1 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 90 (1957), S. 909-921 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclische Iminoäther vom Typ des Caprolactim-methyläthers reagieren leicht mit Acylhydrazinen, insbesondere mit Carbonsäurehydraziden. Dabei bilden sich in erster Stufe „amidrazonartige“ Verbindungen, die unter Wasserabspaltung in 1.2.4-Triazole mit einem in 4.5-Stellung angegliederten Ring übergehen. Die „Amidrazone“ aus cyclischen Lactimäthern und Hydrazin-mono-carbonsäureestern erleiden einen ähnlichen Triazolringschluß, jedoch unter Abspaltung von Alkohol; es bilden sich 3-Hydroxy-triazole. Für diese Arbeiten wurden einige neue cyclische Lactimäther hergestellt.
    Additional Material: 2 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 92 (1959), S. 298-304 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Darstellung der echten Acetobromverbindung des D-Glucosamins (1-α-Brom-N-acetyl-3.4.6-triacetyl-D-glucosamin) (I) wird beschrieben. Diese lagert sich in Gegenwart von Wasser in das bekannte 1.3.4.6-Tetraacetyl-α-D-glucosamin-hydrobromid (VIII) um. Während als Zwischenprodukt bei der Umwandlung des 1-α-Brom-N-benzoyl-Derivates des D-Glucosamins das Salz eines Oxazolinderivates(2) isoliert werden konnte, wurde beim N-Acetyl-Produkt mit einem Überschuß von Bromwasserstoff/Eisessig als kristallines Zwischenprodukt das Salz eines Oxazolidinderivates (III) erhalten. Für letzteres ist auch die Formel eines N-Hydrobromids der Acetobromverbindung (VI) in Betracht zu ziehen. Aus diesem Salz des Oxazolidinderivates entstehen mit Alkoholen Glykoside und mit Pyridin das Pyridiniumsalz VII. Letzteres kann auch aus 1 mit Pyridin erhalten werden.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 90 (1957), S. 521-526 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-1-Chlor-3.4.6-triacetyl-N-acetyl-D-glucosamin (I) wird dargestellt. Es kann in Tetraacetyl-β-D-glucosaminide (III) übergeführt, anderseits zum 1.3.4.6- Tetraacetyl-α-D-glucosamin-hydrochlorid (II) umgelagert werden. Aus 1.3.4.6- Tetraacetyl-N-benzoyl-d-glucosamin (IX) wird das Hydrobromid eines Oxazolinderivates (V) hergestellt und dieses in α-1-Benzoyl-3.4.6-triacetyl-D-glucosamin-hydrobromid (VI) umgelagert.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 3423-3428 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation of Novel 1,2,3-Selenadiazoline SystemsIntroduction of acyl groups to 1 may occur at the four heteroatoms as reactive centres. Although the reaction with acetic acid leads by H⊕ ion catalysis to the corresponding ester 3, an attack at N-2 occurs with acyl chlorides or p-toluenesulfonyl chloride in an alkaline medium. Tricyclic 1,2,3-selenadiazolines 4A are formed. Elucidation of the structure is performed by detailed spectroscopic investigations. Especially valuable for this purpose is the 13C-77 Se coupling in the NMR.
    Notes: Bei der Acylierung von 1 kommen die vier Heteroatome als reaktive Zentren in Betracht. Während die Umsetzung mit Essigsäure unter H⊕-Ionen-Katalyse zur Esterbildung führt (3), erhält man mit Carbonsäurechloriden oder p-Toluolsulfonylchlorid im basischen Medium einen Angriff an N-2. Dabei entstehen die tricyclischen 1,2,3-Selenadiazoline 4A. Die Strukturaufklärung gelingt mit Hilfe eingehender spektroskopischer Untersuchungen. Als besonders wertvoll erweist sich dabei die 13C-77 Se-Kopplung in der Kernresonanz.
    Additional Material: 4 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 1545-1549 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: ThiatriazadiphosphorinePentachlorothiatriazadiphosphorine 2 is formed by the reaction of bis(trimethylsilyl)sulfur diimide and phosphorus pentachloride. With SbCl5 2 yields the complex N3P2Cl4S+SbCl6-(2a). Its structure was elucidated on the basis of an X-ray analysis. 2a crystallizes in the orthorhombic space group Pnma.The cation exhibits a planar six-membered ring with a two-coordinate sulfur atom. The S—N distances were found to be 155.6 and 156.4 pm, respectively(∢ NSN 119.9°).
    Notes: Das Pentachlorthiatriazadiphosphorin 2 bildet sich bei der Reaktion von Bis (trimethylsilyl)schwefeldiimid mit Phosphorpentachlorid. Aus SbCl5 und 2 entsteht der Komplex N3P2Cl4S+SbCl6- (2a), dessen Molekülstruktur durch eine Röntgenstrukturanalyse aufgeklärt wurde. 2a kristallisiert orthorhombisch in der Raumgruppe Pnma. Für das Kation ergibt sich ein planarer Sechsring mit zweifach koordiniertem Schwefel. Die S—N-Abstände wurden zu 155.6 bzw. 156.4 pm bestimmt (∢ NSN 119.9°).
    Additional Material: 1 Ill.
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  • 7
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and X-ray Structure Analysis of the Addition Compound of Sulfurtrioxide and Tetrasulfurtetranitride (S4N4· SO3)S4N4 · SO3 was obtained by reaction of S4N4 with SO3 in CH2Cl2 and by solvent free reaction of S4N4 with Fluorosulfonic acid anhydride. The structure of the adduct could be determined by single crystal X-ray structure analysis. The “cage” of the S4N4 is analogous to the structure of S4N4 · SbCl5 reconvoluted into a deformated saddle conformation with nearly Cs-symmetry. The S—N bond lengths in the S4N4 ring vary from 1.51 to 1.69 Å. The Cs-symmetry is significantly disturbed by the position of the SO3 group. In the crystal structure with monoclinic unit cell of space group P21/n the molecules are packed into columns, which are arranged pseudohexagonally.
    Notes: S4N4 · SO3 wurde durch Reaktion von S4N4 mit SO3 in CH2Cl2 und über eine lösungsmittelfreie Umsetzung von S4N4 mit Fluorsulfonsäureanhydrid erhalten. Eine Einkristall-Röntgen-Strukturanalyse lieferte die Struktur des Adduktes. Der „Käfig“ des freien S4N4 faltet analog der Struktur des S4N4 · SbCl5 in eine deformierte Sattelkonformation mit näherungsweise Cs-Symmetrie um. Die S—N-Bindungsabstände im S4N4-Ring Variieren von 1,51 bis 1,69 Å. Die Cs-Symmetrie wird deutlich durch die Stellung der SO3-Gruppe durchbrochen. In der Kristallstruktur mit einer monoklinen Elementarzelle der Raumgruppe P21/n ordnen sich die Moleküle in Säulen mit pseudohexagonaler gegenseitiger Anordnung.
    Additional Material: 7 Ill.
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  • 8
    Publication Date: 2008-07-18
    Description: Internal brain states form key determinants for sensory perception, sensorimotor coordination and learning. A prominent reflection of different brain states in the mammalian central nervous system is the presence of distinct patterns of cortical synchrony, as revealed by extracellular recordings of the electroencephalogram, local field potential and action potentials. Such temporal correlations of cortical activity are thought to be fundamental mechanisms of neuronal computation. However, it is unknown how cortical synchrony is reflected in the intracellular membrane potential (V(m)) dynamics of behaving animals. Here we show, using dual whole-cell recordings from layer 2/3 primary somatosensory barrel cortex in behaving mice, that the V(m) of nearby neurons is highly correlated during quiet wakefulness. However, when the mouse is whisking, an internally generated state change reduces the V(m) correlation, resulting in a desynchronized local field potential and electroencephalogram. Action potential activity was sparse during both quiet wakefulness and active whisking. Single action potentials were driven by a large, brief and specific excitatory input that was not present in the V(m) of neighbouring cells. Action potential initiation occurs with a higher signal-to-noise ratio during active whisking than during quiet periods. Therefore, we show that an internal brain state dynamically regulates cortical membrane potential synchrony during behaviour and defines different modes of cortical processing.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Poulet, James F A -- Petersen, Carl C H -- England -- Nature. 2008 Aug 14;454(7206):881-5. doi: 10.1038/nature07150. Epub 2008 Jul 16.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Sensory Processing, Brain Mind Institute, Faculty of Life Sciences, Ecole Polytechnique Federale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18633351" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Electroencephalography ; Exploratory Behavior/*physiology ; Male ; Membrane Potentials/*physiology ; Mice ; Mice, Inbred C57BL ; Neurons/*physiology ; Somatosensory Cortex/*physiology ; Wakefulness/*physiology
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 9
    Publication Date: 1978-10-20
    Description: Five Japanese macaques and five other Old World monkeys were trained to discriminate among field-recorded Japanese macaque vocalizations. One task required discrimination of a communicatively relevant acoustic feature ("peak"), and a second required discrimination of an orthogonal feature of the same vocalizations ("pitch"). The Japanese animals more proficiently discriminated the peak feature when stimuli were presented to the right ear (primarily left cerebral hemisphere), as opposed to the left ear (primarily right hemisphere). In discriminating the pitch feature, the Japanese animals either showed (i) a left-ear processing advantage or (ii) no ear advantage. The comparison animals, with one exception, showed no ear advantage in processing either feature of the vocalizations. The results suggest that Japanese macaques engage left-hemisphere processors for the analysis of communicatively significant sounds that are analogous to the lateralized mechanisms used by humans listening to speech.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Petersen, M R -- Beecher, M D -- Zoloth, S R -- Moody, D B -- Stebbins, W C -- New York, N.Y. -- Science. 1978 Oct 20;202(4365):324-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/99817" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Auditory Perception/*physiology ; Discrimination Learning/physiology ; Female ; *Functional Laterality ; Haplorhini ; Macaca/*physiology ; Male ; Species Specificity ; Vocalization, Animal/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 10
    Publication Date: 2019-06-27
    Description: An explicit technique for calculating atmospheric trajectories is presented as an alternative method to the standard implicit scheme of Danielsen (1961). The technique uses the inviscid equations of motion and the discrete model formulation derived by Greenspan (1972, 1973) to compute trajectories on isentropic surfaces, assuming adiabatic flow. The discrete model formulation is designed specifically for a Lagrangian system and objectively accounts for the geostrophic departures, local psi-tendencies, and the subsequent accelerations along the entire length of the trajectory. Application of the discrete formulation to a diagnostic case study yielded favorable results.
    Keywords: METEOROLOGY AND CLIMATOLOGY
    Type: Monthly Weather Review; 107; May 1979
    Format: text
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