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Simon, Robert C.; Grischek, Barbara; Zepeck, Ferdinand; Steinreiber, Andreas; Belaj, Ferdinand; Kroutil, Wolfgang
Angewandte Chemie (International ed.), July 2, 2012, Letnik: 51, Številka: 27Journal Article
Hitting the right target: Differentiation between two keto moieties was accomplished by a regio‐ and enantioselective bioamination employing ω‐transaminases. Using 1,5‐diketones as substrates gave access to the optically pure 2,6‐disubstituted piperidine scaffold. The approach allowed the shortest synthesis of the alkaloid dihydropinidine, as well as its enantiomer, by choosing an appropriate ω‐transaminase.
