| Literature DB >> 22887645 |
Johann H Sattler1, Michael Fuchs, Katharina Tauber, Francesco G Mutti, Kurt Faber, Jan Pfeffer, Thomas Haas, Wolfgang Kroutil.
Abstract
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. 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.Entities:
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Year: 2012 PMID: 22887645 DOI: 10.1002/anie.201204683
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336