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  • 1
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 23 (1984), S. 1487-1489 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 25 (1986), S. 3879-3883 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 45 (1980), S. 1713-1715 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 50 (1985), S. 2416-2423 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 24 (1994), S. 311-314 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The molecular and crystal structure of the title compound2, prepared in racemic form by addition of phenylmagnesium bromide to 6-exo-methyl-6-endo-nitrobicyclo[2.2.1]heptan-2-one (1) in the presence of cerium(III) chloride, were determined by single-crystal X-ray diffraction. The crystal selected for analysis was found to belong to the chiral orthorhombic space group P212121, witha=6.685(3),b=10.0788(5),c=18.581(1) Å. In the crystal, molecules of2 are associated by intermolecular hydrogen bonds between hydroxy and nitro groups (OH...O2N=0.82 Å).
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 865-870 
    ISSN: 1434-193X
    Keywords: Alkaloids ; Enaminones ; Indolizidines ; Sulfide contraction ; Total synthesis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of the racemic title alkaloid 1 has been accomplished in eight steps and 7.2% overall yield from pyrrolidine-2-thione (5) and ethyl hex-2-enoate (6). Key steps include a ring closure that takes advantage of the nucleophilicity of a vinylogous urethane 8, and stereoselective reduction of the C=C double bond of a bicyclic vinylogous amide 12.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 105 (1993), S. 1-24 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Das Meer ist eine scheinbar unerschöpfliche Quelle für Organismen, deren Sekundärmetaboliten Zeugnis ablegen von dem Erfindungsreichtum, mit dem die Natur den molekularen Aufbau verändert. Aber zu welchem Zweck werden diese vielfältigen und oft eigenartigen Verbindungen produziert? Wir sind der Meinung, daß einige von ihnen an der Aufnahme und dem Transport der in wäßrigem Milieu vorhandenen Metall-Ionen beteiligt sein könnten. Während man von vielen durch Landlebewesen produzierten Metaboliten weiß, daß sie als Ionophore dienen können, ist über ein ähnliches Verhalten ihrer marinen Analoga weit weniger bekannt. Ungeachtet der relativen Häufigkeit bestimmter Metall-Ionen in den Ozeanen und von Metabolitstrukturen, die eine Chelatbildung mit Metall-Ionen erleichtern sollten, wurden nur wenige Versuche gemacht, eine Verbindung zwischen diesen beiden Phänomenen herzustellen. Wir haben aus der umfangreichen Literatur über die von Meereslebewesen produzierten Naturstoffe die ausgewählt, die für unsere Prämisse wesentliche Beobachtungen und Vermutungen enthält, und werten diese im folgenden aus. Lediglich eine Handvoll metallhaltiger Komplexe wurde tatsächlich isoliert; außerdem sind Versuche selten, solche Komplexe in vitro herzustellen, und spektroskopische Hinweise auf Metall-Metabolit-Wechselwirkungen sind weder in vivo noch in vitro häufig. Nur bei den vanadiumhaltigen Tunichromen beginnt sich eine plausible (aber keineswegs vollständige) Vorstellung zu entwickeln. In mehreren anderen Fällen wird die Wahrscheinlichkeit einer Metallkomplexierung - obwohl von den Autoren diskutiert - durch experimentelle Hinweise nicht gestützt. Die Bemühungen, Informationen über die Struktur und insbesondere die Konformation der Metaboliten durch Röntgenkristallographie, NMR-Spektroskopie und Molekülmechanikrechnungen zu erhalten, scheinen jedoch den Schlüssel für einen rationalen Zugang zu diesem vernachlässigten Thema zu liefern. Ausgehend von neueren Studien über strukturelle Aspekte von marinen Metaboliten stellen wir eine Auswahl der Verbindungen vor, deren Potential zur Bindung von Metall-Ionen weitere Untersuchungen verdient und von denen einige Ziel unserer Synthesebemühungen sind.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 32 (1993), S. 1-23 
    ISSN: 0570-0833
    Keywords: Metabolism ; Chelates ; Natural products ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The marine environment is a seemingly inexhaustible treasury of organisms whose secondary metabolites bear witness to the lavishness and inventiveness with which nature is able to manipulate molecular architecture. But to what purpose are these diverse and often grotesque compounds produced? This review is founded on the premise that some of them may be involved in the uptake and transport of metal ions present in the aquatic milieu. Many metabolites produced by terrestrial organisms are known to act as ionophores, but the case for similar behavior by their marine counterparts is far hazier. Notwithstanding the relative abundance of certain metal ions in the oceans, and of metabolite structures possessing features that should facilitate the chelation of metal ions, few attempts to establish a connection between these two phenomena have been reported. We have whittled down the voluminous literature of natural products derived from marine sources to expose a core of observations and speculations germane to our premise. These facts and fantasies are evaluated in this review. A mere handful of metal-containing complexes has actually been isolated; furthermore, attempts to prepare such complexes in vitro are rare, and spectroscopic evidence for metal-metabolite interactions, whether in vivo or in vitro, is not common. Only with the vanadium-sequestering tunichromes does a logical (but by no means complete) picture begin to emerge. In several other cases, the plausibility of metal chelation, though mooted by authors, remains unsupported by experimental evidence. However, continuing efforts to obtain structural, and particularly conformational, information on the metabolites by means of X-ray crystallography, nuclear magnetic resonance spectroscopy, and molecular mechanics calculations would seem to provide the key to a rational approach to this neglected topic. On the basis of recent studies dealing with such structural aspects, we present a selection of candidate compounds, some of which are the targets of our own synthetic attentions, whose potential for binding to metal cations merits further research.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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