3 results match your criteria: "Institute of Organic Chemisty[Affiliation]"
The first general, efficient and highly enantioselective reduction of quinoxalines and quinoxalinones.
Chemistry
March 2010
Institute of Organic Chemisty, RWTH Aachen, Landoltweg 1, 52074 Aachen, Germany.
Synthesis of rigidified flavin-guanidinium ion conjugates and investigation of their photocatalytic properties.
Beilstein J Org Chem
May 2009
Institute of Organic Chemisty, University of Regensburg, Universitätsstr. 31, D-93040 Regensburg, Germany.
Flavin chromophores can mediate redox reactions upon irradiation by blue light. In an attempt to increase their catalytic efficacy, flavin derivatives bearing a guanidinium ion as oxoanion binding site were prepared. Chromophore and substrate binding site are linked by a rigid Kemp's acid structure.
View Article and Find Full Text PDFAsymmetric Brønsted acid catalysis: enantioselective nucleophilic substitutions and 1,4-additions.
Angew Chem Int Ed Engl
February 2008
Institute of Organic Chemisty and Chemical Biology, Johann Wolfgang Goethe-Universität Frankfurt am Main, Max-von-Laue Strasse 7, 60438 Frankfurt am Main, Germany.