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  • Publication
    Accès libre
    The Stereochemistry of the 1,4-Elimination of Thiocyanic Acid from Hex-3-ene-2,5-diyl Dithiocyanates
    (1993)
    Schoepfer, Joseph
    ;
    Eichenberger, Eugen
    ;
    The elimination of thiocyanic acid from the stereoisomers of the hex-3-ene-2,5-diyl dithiocyanates, 4a, 4b, 6a and 6b, in the presence of a strong neutral base in an organic solvent, yields mixtures of the hex-2,4-dien-2-yl thiocyanates 9, 10 and 11via a preferentially syn process.
  • Publication
    Accès libre
    Photophysics and photochemistry of 4-Dihydropyridinones
    (1990)
    Aeby D.
    ;
    Eichenberger, Eugen
    ;
    Haselbach, E.
    ;
    Suppan, P.
    ;
    Guerry, Philippe
    ;
    Dihydropyridinones (DHP) react photochemically with olefins to form cycloaddition products. The reactions proceed through the lowest excited state T, of the DHPs, with rate constants which depend on the olefin and can approach the diffusional limit in the most favourable cases. Intra- and inter-molecular sensitization and quenching have been investigated, as well as spectroscopic properties such as absorption and luminescence spectra, and in particular electron energy loss spectra which have established the energy of the reactive T, state as 295 kJ mol"' (3.07 eV).