@misc{LemkeFernandezTrujilloLoehmannsroeben2005,
  author    = {Lemke, Matthias and Fern{\´a}ndez-Trujillo, Rebeca and L{\"o}hmannsr{\"o}ben, Hans-Gerd},
  title     = {In-situ LIF analysis of biological and petroleum-based hydraulic oils on soil},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-12268},
  year      = {2005},
  abstract  = {Absorption and fluorescence properties of 4 hydraulic oils (3 biological and 1 petroleum-based) were investigated. In-situ LIF (laser-induced fluorescence) analysis of the oils on a brown sandy loam soil was performed. With calibration, quantitative detection was achieved. Estimated limits of detection were below ca. 500 mg/kg for the petroleum-based oil and ca. 2000 mg/kg for one biological oil. A semi-quantitative classification scheme is proposed for monitoring of the biological oils. This approach was applied to investigate the migration of a biological oil in soil-containing compartments, namely a soil column and a soil bed.},
  language  = {en}
}
@misc{SchmidtHauke2013,
  author    = {Schmidt, Bernd and Hauke, Sylvia},
  title     = {Cross metathesis of allyl alcohols},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-95037},
  pages     = {4194 -- 4206},
  year      = {2013},
  abstract  = {Under standard conditions the cross metathesis of allyl alcohols and methyl acrylate is accompanied by the formation of ketones, resulting from uncontrolled and undesired double bond isomerization. By conducting the CM in the presence of phenol, the catalyst loading and the reaction time required for quantiative conversion can be reduced, and isomerization can be suppressed. On the other hand, consecutive isomerization can be deliberately promoted by evaporating excess methyl acrylate after completing cross metathesis and by adding a base or silane as chemical triggers.},
  language  = {en}
}