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Maschinen in Gang gebracht: Eine biokatalytische redoxneutrale Kaskade zur Herstellung terminaler primärer Amine aus primären Alkoholen und Ammoniak wurde in einer einstufigen Eintopfreaktion entwickelt (siehe Bild). Mit dem künstlichen biokatalytischen Netzwerk wurden langkettige 1,ω‐Alkandiole bei einem Umsatz von bis zu 99 % in Diamine umgewandelt.
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