172,221 research outputs found

    Aussreden und Fürwort der loblichen Büchsenschützen : darinnen allerhand Ursachen und zuofallende Gelegenheiten so im Schiessen fürfallen, auch in was Gstalten sich die zutragen mögen, erzelt unnd beschriben werden : gantz kurtzwylig und den Schützen sonderlich nutzlich zuläsen

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    gestelt zu Ehren und Wollgefallen der loblichen Geselschafft der Büchsenschützen der uralten Statt und Landschafft Zürych [von Hans Heinrych Grob d. jünger.]Bogensignaturen: A-C⁴, D⁶Titelvignette, kolorier

    Aussreden und Fürwort der loblichen Büchsenschützen : darinnen allerhand Ursachen und zuofallende Gelegenheiten so im Schiessen fürfallen, auch in was Gstalten sich die zutragen mögen, erzelt unnd beschriben werden : gantz kurtzwylig und den Schützen sonderlich nutzlich zuläsen

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    gestelt zu Ehren und Wollgefallen der loblichen Geselschafft der Büchsenschützen der uralten Statt und Landschafft Zürych [von Hans Heinrych Grob d. jünger.]Bogensignaturen: A-C⁴, D⁶Titelvignette, kolorier

    [Christoph Heinrich Grob]

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    Kniestück, stehend, im rechten Hintergrund Feder und andere SchreibutensilienCFJrminger ft 1852Unten Mitte mit Bleistift bezeichnet "Christoph Heinrich Grob / Bankkassier" Exemplar der Zentralbibliothek Zürich, Graphische Sammlung und Fotoarchi

    Cygnus evangelicus, historiam doctorum ecclesiae Christi, inde a reformatione, adversum Romani Vulturis et omnis volucris invisae molitiones, prosopopoeia heroica quam brevissime & planissime exprimens

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    auctore Ioanne Huldrycho Grobio Tig., ad clarissimum virum D. Ioannem Guiilielmum Stuckium Theologum TigurinumBogensignaturen: A-C⁴Vermuteter Drucker: Hans Rudolf Wyssenbac

    P. Grelot et C. Bigaré, Introduction à la Bible, tome III, Le Nouveau Testament, vol. 5, L'achèvement des Ecritures, Paris, Desclée, 1977

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    Grob Francis. P. Grelot et C. Bigaré, Introduction à la Bible, tome III, Le Nouveau Testament, vol. 5, L'achèvement des Ecritures, Paris, Desclée, 1977. In: Revue d'histoire et de philosophie religieuses, 60e année n°2, Avril-juin 1980. pp. 227-228

    Going Beyond Counting First Authors in Author Co-citation Analysis

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    The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed

    Approaches towards the synthesis of 7-halo-1,2-dihydroxyindolizidines (7-halolentiginosines) thwarting Grob fragmentation processes

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    The synthesis of 7-halo-1,2-dihydroxyindolizidines (7-halolentiginosines) starting from suitable protected 1,2,7-trihydroxyindolizidines (7-hydroxylentiginosines) has been studied. The results indicate a high propensity of the substrates to undergo fragmentation processes under standard halogenations conditions. The analysis of the products allowed an unprecedented full rationalization of Grob fragmentations processes in 7-substituted 1,2-alkoxyindolizidines. Under optimized Appel reaction conditions 7-chloro- and 7-iodolentiginosines could be exclusively achieved (89e100% yields), whereas fluoruration was extremely sluggish and the 7-fluoro derivative was formed in only 19% through a twostep protocol. Biological assays proved that 7-fluoro- and 7-iodolentiginosines are endowed with proapoptotic activity analogously to ()-lentiginosine and 7-hydroxylentiginosine
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