Biomimetic Explorations Towards the Bisorbicillinoids: Total Synthesis of Bisorbicillinol, Bisorbibutenolide, and Trichodimerol

Strikingly simple cascade dimerization sequences can be used to assemble the complex frameworks of bisorbicillinoids such as bisorbicillinol (1), bisorbibutenolide (2), and trichodimerol (3). The mechanistic facets of the biomimetic total syntheses of these bioactive natural products were also explored. Inspection of the unique molecular architecture of these compounds reveals that they are likely to be assembled in nature by a dimerization of two oxidized forms of sorbicillin.     

Darstellung und Eigenschaften einiger neuer Arsenat- und Vanadat-Halogen-Apatite

Preparation and Properties of Some New Arsenate and Vanadate Halogen Apatites The preparation of new apatite-like compounds of the composition Na₂Nd₂Pb₆(RO₄)₆X₂ (with R = As, V and X = Cl, Br and also R = P and X = Br) is reported. Crystallographic data for these as well as for the already known Na₂Nd₂Pb₆(PO₄)₆Cl₂ are determined from the corresponding X-ray powder diagrams. Also the infrared and Raman spectra were recorded and briefly discussed.     

Abschätzung mittlerer Schwingungsamplituden der Metall—Sauerstoff-Bindungen einiger Hexaoxometallate

Mean amplitudes of vibration of a series of hexaoxometalates have been estimated using an approximation method and recently reported spectroscopic data arising from the study of the respective lithium salts.     

$\delta$-pairing forces and collective pairing vibrations

The collective pairing Hamiltonian is obtained in the framework of the generator coordinate method in the Gaussian overlap approximation with a slightly modified BCS function used as a generator function. The collective variable , measuring the monopole moment of the pairing field, and the gauge transformation angle are chosen as generator coordinates. The vibrational ground states are calculated by diagonalisation of the collective pairing Hamiltonian in the harmonic-oscillator basis.Received: 28 April 2003, Revised: 1 October 2003, Published online: 18 June 2004PACS: 21.30.-x Nuclear forces - 21.60.Ev Collective models     

Isolation and characterization of kallosin A,a novel rearranged pseudopterane diterpenoid from the Caribbean sea plume Pseudopterogorgia kallos (Bielschowsky)

The Caribbean alcyonacean Pseudopterogorgia kallos is shown to contain a novel rearranged pseudopterane diterpene, kallosin A (1), possessing several unusual structural features. In addition to having two distinct 2(3H)- and 2(5H)-furanone moieties, kallosin A is based on a new carbon skeleton. The structural assignment of 1 was based mainly on 1D and 2D NMR spectral data and was further supported by accurate mass measurement and single-crystal X-ray diffraction analysis.