Publication | Closed Access
A Base‐Promoted Tandem Reaction of 3‐(1‐Alkynyl)chromones with 1,3‐Dicarbonyl Compounds: An Efficient Approach to Functional Xanthones
57
Citations
25
References
2009
Year
Asymmetric CatalysisBase‐promoted Tandem ReactionEngineeringAlkene MetathesisFunctionalized XanthonesTransition-metal CatalystEfficient ApproachOrganic ChemistryOrganometallic CatalysisCatalysisChemistryFunctional XanthonesHeterocycle ChemistryPharmacologyTandem ProcessSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
No need for a transition-metal catalyst is characteristic for the tandem process presented herein to obtain functionalized xanthones. The sequence involves multiple reactions, such as Michael addition-elimination/cyclization/1,2-addition/elimination reactions (see scheme).
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