Aerobic oxidation of isosorbide and isomannide employing TEMPO/laccase
The oxidation of the renewable diols isosorbide and isomannide was successfully achieved using a TEMPO/laccase system. Furthermore, various TEMPO-derivatives were tested leading to conversions of up to >99% for the oxidation of isosorbide, isomannide, indanol and a halohydrin to the corresponding...
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Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2014-01, Vol.16 (4), p.2117-2121 |
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container_title | Green chemistry : an international journal and green chemistry resource : GC |
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creator | Gross, Johannes Tauber, Katharina Fuchs, Michael Schmidt, Nina G. Rajagopalan, Aashrita Faber, Kurt Fabian, Walter M. F. Pfeffer, Jan Haas, Thomas Kroutil, Wolfgang |
description | The oxidation of the renewable diols isosorbide and isomannide was successfully achieved using a TEMPO/laccase system. Furthermore, various TEMPO-derivatives were tested leading to conversions of up to >99% for the oxidation of isosorbide, isomannide, indanol and a halohydrin to the corresponding ketone. |
doi_str_mv | 10.1039/C3GC41855C |
format | Article |
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title | Aerobic oxidation of isosorbide and isomannide employing TEMPO/laccase |
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