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Dr. Wolf-Dieter Fessner, Dipl.-Chem. Gudrun Sinerius, Dipl.-Chem. Achim Schneider, Dipl.-Chem. Matthias Dreyer, Prof. Dr. Georg E. Schulz, Dr. Josefa Badia and Prof. Dr. Juan Aguilar Diastereoselective Enzymatic Aldol Additions: L-Rhamnulose and L-Fuculose 1-Phosphate Aldolases from E. coli Angewandte Chemie International Edition in English 30

Article first published online: 22 DEC 2003 | DOI: 10.1002/anie.199105551

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Two bacterial aldolases, RhuA and FucA, which are readily accessible by overex-pression, catalyze the asymmetric addition of dihydroxyacetone phosphate to various aldehydes. The high degree of enantio-and diastereoselectivity for the L-threo (RhuA) and D-erythro (FucA) stereochemistry of the products and the high stability of the enzymes make it possible to prepare rare carbohydrates and their derivatives as well as other polyhydroxylated compounds.

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