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Diastereoselective Tin-Free Tandem Radical Additions to 3-Formylchromones
11
Citations
36
References
2011
Year
Medicinal ChemistryNatural SciencesRadical (Chemistry)Molecular BiologyOrganic ChemistryOrganometallic CatalysisSynthetic ChemistryStereoselective SynthesisChemistryHeterocycle ChemistryAsymmetric CatalysisContiguous StereocentersCarbon-carbon Bond-forming StepsChromone Structures
A tin-free tandem radical addition methodology onto 3-formylchromones is presented. This radical process yields functionalized chromone structures via two carbon-carbon bond-forming steps. These products contain up to three contiguous stereocenters with good to excellent dr's and yields.
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