897 research outputs found

    Involvement of titanocene and related species in the reduction of dinitrogen and olefins

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    Journal ArticleSummary Four sequential products have been spectrally detected in the reduction by sodium of dicyclopentadienyltitanium(iv) dichloride: [(77-Cp)2TiCl]2, [(77-Cp)2-Ti]1-2, [(77-Cp)(C5H4)TiH]x, and (77-Cp)(C5H4)TiH2Ti- (C5H4)(77-Cp) ("stable titanocene"); the second of these reacts rapidly and reversibly with N2 to give a dark blue complex reducible to ammonia and appears to catalyse the cyclopentadienyltitanium-promoted rapid, room temperature-atmospheric pressure hydrogenation of olefins

    Two Antimycin A Analogues from Marine-Derived Actinomycete Streptomyces lusitanus

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    Two new antimycin A analogues, antimycin B1 and B2 (1–2), were isolated from a spent broth of a marine-derived bacterium, Streptomyces lusitanus. The structures of 1 and 2 were established on the basis of spectroscopic analyses and chemical methods. The isolated compounds were tested for their anti-bacterial potency. Compound 1 was found to be inactive against the bacteria Bacillus subtilis, Staphyloccocus aureus, and Loktanella hongkongensis. Compound 2 showed antibacterial activities against S. aureus and L. hongkongensis with MIC values of 32.0 and 8.0 μg/mL, respectively

    Gram-Scale Synthesis of the (-)-Sparteine Surrogate and (-)-Sparteine

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    An 8-step, gram-scale synthesis of the (-)-sparteine surrogate (22% yield, with just 3 chromatographic purifications) and a 10-step, gram-scale synthesis of (-)-sparteine (31% yield) are reported. Both syntheses proceed with complete diastereocontrol and allow access to either antipode. Since the syntheses do not rely on natural product extraction, our work addresses long-term supply issues relating to these widely used chiral ligands

    Alkylwanderungen bei Sextettumlagerungen

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    Die Wanderungstendenzen von Alkylgruppen bei der Beckmann- Criegee- und Isonitril-Nitril-Umlagerung werden untersucht. Aus den relativen Reaktionsgeschwindigkeiten der substituierten Benzylreste werden Rückschlüsse auf die Ladungsverteilung im Übergangszustand dieser Reaktionen gezogen und aus dem Verhältnis der Wanderungstendenzen des exo und endo- 2- Norbornylrestes auf die Geometrie der wandernden Gruppe im Übergangszustand. Der in verschiedenen Sextettumlagerungen unterschiedliche Einfluß der -Methylverzweigung in der wandernden Gruppe wird interpretiert
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