Asymmetric Synthesis of (R)‐1‐Alkyl‐Substituted Tetrahydro‐ß‐carbolines Catalyzed by Strictosidine Synthases |
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Authors: | Dr Desiree Pressnitz Dr Eva‐Maria Fischereder Dr Jakob Pletz Christina Kofler Lucas Hammerer Katharina Hiebler Dr Horst Lechner Dr Nina Richter Elisabeth Eger Prof?Dr Wolfgang Kroutil |
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Institution: | 1. Department of Chemistry, Organic und Bioorganic Chemistry, University of Graz, NAWI Graz, BioTechMed Graz, Graz, Austria;2. ACIB GmbH—Austrian Center of Industrial Biotechnology, Graz, Austria |
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Abstract: | Stereoselective methods for the synthesis of tetrahydro‐ß‐carbolines are of significant interest due to the broad spectrum of biological activity of the target molecules. In the plant kingdom, strictosidine synthases catalyze the C?C coupling through a Pictet–Spengler reaction of tryptamine and secologanin to exclusively form the (S)‐configured tetrahydro‐ß‐carboline (S)‐strictosidine. Investigating the biocatalytic Pictet–Spengler reaction of tryptamine with small‐molecular‐weight aliphatic aldehydes revealed that the strictosidine synthases give unexpectedly access to the (R)‐configured product. Developing an efficient expression method for the enzyme allowed the preparative transformation of various aldehydes, giving the products with up to >98 % ee. With this tool in hand, a chemoenzymatic two‐step synthesis of (R)‐harmicine was achieved, giving (R)‐harmicine in 67 % overall yield in optically pure form. |
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Keywords: | asymmetric catalysis biocatalysis Pictet– Spengler reaction strictosidine Synthases tetrahydro-β -carbolines |
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