Abstract
Levulinic acid and its esters participate in transfer hydrogenation with a range of secondary alcohols. Reduction of the levulinate leads to cyclisation into a gamma-lactone, thereby acting as an oxidant for alcohols without the need for a large excess of reagents. (c) 2007 Elsevier Ltd. All rights reserved.
Original language | English |
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Pages (from-to) | 3639-3641 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 48 |
Issue number | 21 |
DOIs | |
Publication status | Published - 2007 |