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Synlett 2014; 25(1): 1-7
DOI: 10.1055/s-0033-1340153
DOI: 10.1055/s-0033-1340153
synpacts
Total Synthesis of (+)-Fusarisetin A: A Biomimetic Approach
Weitere Informationen
Publikationsverlauf
Received: 26. August 2013
Accepted after revision: 17. September 2013
Publikationsdatum:
05. November 2013 (online)
Abstract
This article outlines our recent efforts to synthesize (+)-fusarisetin A, a naturally occurring 3-acyltetramic acid, by a route based on a hypothetical biosynthesis. Our research suggests that the biosynthesis of (+)-fusarisetin A might involve the aerobic oxidation of equisetin, possibly mediated by metal oxidants or by photochemically produced reactive oxygen species.
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For atom-economic synthesis, see:
For step-economic synthesis, see:
For redox-economic synthesis, see:
For total syntheses of fusarisetin A, see:
For a review on progress in the synthesis of fusarisetin A, see:
For the isolation of equisetin, see:
For reviews on the Diels–Alder reaction in total synthesis, see:
For a review on intramolecular Diels–Alder reactions in total synthesis, see:
For total syntheses of equisetin, see:
For reviews on Mn(III)-promoted radical reactions, see:
For a review on the mechanisms of Mn(OAc)3-based radical reactions, see: