Publication | Closed Access
Catalytic Asymmetric Cycloadditions between Aldehydes and Enolizable Anhydrides: <i>cis</i>-Selective Dihydroisocoumarin Formation
13
Citations
37
References
2018
Year
EngineeringOrganic ChemistryChemistryDft StudyCatalytic Asymmetric CycloadditionsOrganometallic CatalysisStereoselective SynthesisGlutaconic Anhydride DerivativesBiochemistryAryl SuccinicCatalysisPharmacologyAsymmetric CatalysisNatural Product SynthesisEnantioselective SynthesisBiomolecular EngineeringEnolizable AnhydridesNatural SciencesSynthetic Chemistry
In the presence of a trityl-substituted cinchona alkaloid-based catalyst, homophthalic, aryl succinic, and glutaconic anhydride derivatives reacted with aromatic and aliphatic aldehydes to produce cis-lactones in up to 90:10 dr and 99% ee. A DFT study has shown how the catalyst is uniquely able to bring about the opposite sense of diastereocontrol to that usually observed.
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