Publication | Closed Access
Asymmetric Construction of Highly Functionalized Spirobarbiturate‐Cyclopentenes through Chiral Phosphine‐Catalyzed [3+2] Annulation of Morita–Baylis–Hillman Carbonates with Barbiturate‐Derived Alkenes
58
Citations
77
References
2016
Year
Chiral Spirobarbiturate‐cyclopentenesAsymmetric CatalysisChemical EngineeringEngineeringHighly Functionalized Spirobarbiturate‐cyclopentenesExcellent YieldsMild ConditionsOrganic ChemistryCatalysisChemistryAsymmetric ConstructionChiral Phosphine‐catalyzedSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Abstract A multifunctional chiral phosphine‐catalyzed enantioselective [3+2] annulation of Morita–Baylis–Hillman carbonates with barbiturate‐derived alkenes has been achieved under mild conditions, providing a variety of chiral spirobarbiturate‐cyclopentenes in moderate to excellent yields with moderate to excellent diastereo‐ and enantioselectivities. magnified image
| Year | Citations | |
|---|---|---|
Page 1
Page 1