E-viri
Recenzirano
-
Sattler, Johann H.; Fuchs, Michael; Tauber, Katharina; Mutti, Francesco G.; Faber, Kurt; Pfeffer, Jan; Haas, Thomas; Kroutil, Wolfgang
Angewandte Chemie (International ed.), September 3, 2012, Letnik: 51, Številka: 36Journal Article
Driving the machinery: A biocatalytic redox‐neutral cascade for the preparation of terminal primary amines from primary alcohols at the expense of ammonia has been established in a one‐pot one‐step method (see picture). Applying this artificial biocatalyst network, long‐chain 1,ω‐alkanediols were converted into diamines, which are building blocks for polymers, in up to 99 % conversion.
