Global ETD Search

Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.

Results

Showing 1 to 3 of 3 for “"benzoin reaction"”.

  1. Neue chirale Triazoliumsalze in der Carben-katalysierten intramolekularen gekreuzten Benzoin-Reaktion

    In nature many metal free catalytic reactions are accomplished in enzymes. The broad facilities of organocatalysis as a selective and environment-friendly synthetic method has only been recognized recently by chemists. This thesis deals with the synthesis of novel chiral polycylic triazolim salts …

    aachen Repository record for Neue chirale Triazoliumsalze in der Carben-katalysierten intramolekularen gekreuzten Benzoin-Reaktion (opens in a new tab)

  2. Entwicklung von Carben-katalysierten asymmetrischen intermolekularen Stetter-Reaktionen und direkt gekreuzter intermolekularer Benzoin-Reaktionen

    … in the asymmetric intermolecular Stetter reaction. The resulting 1,4-diketones were obtained in moderate to excellent yields (49-98%) and good enantioselectivities (56-78% ee). For several Stetter products the enantiomeric excess could be enhanced by a single recrystallization up to 99% …

    aachen Repository record for Entwicklung von Carben-katalysierten asymmetrischen intermolekularen Stetter-Reaktionen und direkt gekreuzter intermolekularer Benzoin-Reaktionen (opens in a new tab)

  3. Neue Heterazoliumsalze aus Prolin und Pyroglutaminsäure und Anwendungen in Carben-katalysierten asymmetrischen nucleophilen Acylierungen

    … that the catalytically active species of these reactions is a nucleophilic carbene. Consequently, enzyme mimetic asymmetric catalytic processes that are mediated by nucleophilic carbenes in vitro as, for instance, the benzoin condensation, the Stetter and other related nucleophilic acylation …

    aachen Repository record for Neue Heterazoliumsalze aus Prolin und Pyroglutaminsäure und Anwendungen in Carben-katalysierten asymmetrischen nucleophilen Acylierungen (opens in a new tab)