@phdthesis{Geissler2011, author = {Geißler, Diana}, title = {Synthese funktionalisierter Furane durch Acrylatmethese und {\"U}bergangsmetall-katalysierte C-C- Verkn{\"u}pfungsreaktionen}, address = {Potsdam}, pages = {159 S.}, year = {2011}, language = {de} } @article{GeisslerButlinHilletal.2008, author = {Geißler, Daniel and Butlin, Nathaniel G. and Hill, Diana and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Hildebrandt, Niko}, title = {Multiplexed diagnostics and spectroscopic ruler applications with terbium to quantum dots FRET}, issn = {1605-7422}, year = {2008}, language = {en} } @article{SchmidtGeissler2011, author = {Schmidt, Bernd and Geissler, Diana}, title = {Olefin-Metathesis-Based Synthesis of Furans by an RCM/Deprotonation/Phosphorylation Sequence and Their Diels-Alder Reactions}, series = {European journal of organic chemistry}, journal = {European journal of organic chemistry}, number = {35}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1434-193X}, doi = {10.1002/ejoc.201101078}, pages = {7140 -- 7147}, year = {2011}, abstract = {Butenolides, obtained by ring-closing metathesis (RCM) of acrylates, undergo quantitative deprotonation with amide bases. Trapping of the resulting anions with electrophiles, for example, chlorophosphates, give furans. Subsequent DielsAlder reaction and acid-catalysed rearrangement of the resulting oxabicyclonorbornadienes give substituted benzenes.}, language = {en} } @article{SchmidtGeissler2011, author = {Schmidt, Bernd and Geissler, Diana}, title = {Ru- and Pd-Catalysed Synthesis of 2-Arylfurans by One-Flask Heck Arylation/Oxidation}, series = {European journal of organic chemistry}, journal = {European journal of organic chemistry}, number = {25}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1434-193X}, doi = {10.1002/ejoc.201100549}, pages = {4814 -- 4822}, year = {2011}, abstract = {2,5-Disubstituted furans were synthesized by one-flask Heck arylation/oxidation sequences. The starting materials are 2-substituted 2,3-dihydrofurans, conveniently available by RCM/isomerization sequences, and arenediazonium salts. These react in ligand-free Heck reactions to afford 2,5-disub-stituted 2,5-dihydrofurans, which are oxidized to the corresponding furans without isolation or intermediate workup. The oxidation is conveniently achieved with chloranil or DDQ, depending on the substrate.}, language = {en} } @misc{ArnoldCaprezDenzetal.2013, author = {Arnold, Rafael and Caprez, Nina F. and Denz, Rebekka and Moreno, Aitor Garc{\´i}a and Geißler-Gr{\"u}nberg, Anke and Gr{\"o}zinger, Elvira and Guttstadt, Corry and Haußig, Hans-Michael and Hiscott, William and K{\"u}hne, Jan and Liebl, Christina and Malkhasy, Hayim and Martini, Annett and Matut, Diana and Quintana, Aldina and Rasumny, Wiebke and Rebiger, Bill and Refael, Shmuel and Ristau, Daniel and Salzer, Dorothea M. and Schmid, Beatrice and Schulte, Christoph}, title = {PaRDeS : Zeitschrift der Vereinigung f{\"u}r J{\"u}dische Studien e.V. = Galut Sepharad in Aschkenas : Sepharden im deutschsprachigen Kulturraum}, number = {19}, publisher = {Universit{\"a}tsverlag Potsdam}, address = {Potsdam}, isbn = {978-3-86956-253-7}, issn = {1614-6492}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-65270}, year = {2013}, abstract = {Die Zeitschrift m{\"o}chte die fruchtbare und facettenreiche Kultur des Judentums sowie seine Ber{\"u}hrungspunkte zur Umwelt in den unterschiedlichen Bereichen dokumentieren. Daneben dient die Zeitschrift als Forum zur Positionierung der F{\"a}cher J{\"u}dische Studien und Judaistik innerhalb des wissenschaftlichen Diskurses sowie zur Diskussion ihrer historischen und gesellschaftlichen Verantwortung.}, language = {de} }