Publication | Closed Access
Singlet-Oxygen-Mediated One-Pot Synthesis of 3-Keto-tetrahydrofurans from 2-(β-Hydroxyalkyl) Furans
46
Citations
16
References
2008
Year
1,4-Enedione IntermediateEngineeringPhotoredox ProcessPhotochemistryBiochemistrySinglet-oxygen-mediated One-pot SynthesisSynthetic OperationMechanistic Photochemistry3-Keto-tetrhydrofuran MotifsSynthetic PhotochemistryOrganic ChemistryNatural Product SynthesisEnantioselective SynthesisBiomolecular Engineering
Photooxygenation of 2-(beta-hydroxyalkyl) furans affords, in one synthetic operation and in high yields, 3-keto-tetrhydrofuran motifs via intramolecular Michael-type addition to the 1,4-enedione intermediate.
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