Publication | Closed Access
Asymmetric Synthesis of Cyclopenta[3,4]pyrroloindolones <i>via N</i>-Heterocyclic Carbene-Catalyzed Michael/Aldol/Lactamization Cascade Reaction
39
Citations
75
References
2017
Year
Asymmetric CatalysisExcellent EnantioselectivityEngineeringHeterocyclicNatural SciencesDiversity-oriented SynthesisAsymmetric SynthesisConsecutive Stereogenic CentersOrganic ChemistryStereoselective SynthesisChemistryHeterocycle ChemistryPharmacologyIndole-derived EnonesSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The N-heterocyclic carbene-catalyzed asymmetric Michael/aldol/lactamization cascade reaction of enals and indole-derived enones for the synthesis of functionalized cyclopenta[3,4]pyrroloindolones with four consecutive stereogenic centers has been achieved. The products were obtained in good yield with high diastereoselectivity and excellent enantioselectivity.
| Year | Citations | |
|---|---|---|
Page 1
Page 1