Publication | Closed Access
Enantioselective [3 + 2] annulation of 4-isothiocyanato pyrazolones and alkynyl ketones under organocatalysis
18
Citations
43
References
2021
Year
4-Isothiocyanato PyrazolonesNovel OrganocatalystsEngineeringHeterocyclicVarious Electronic PropertiesCinchona AlkaloidOrganic ChemistryOrganic CatalystStereoselective SynthesisChemistryHeterocycle ChemistryPharmacologyAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringAlkynyl KetonesNatural Product Synthesis
An asymmetric [3 + 2] annulation reaction of 4-isothiocyanato pyrazolones with alkynyl ketones in the presence of an organic catalyst derived from a cinchona alkaloid under mild conditions is realized. This protocol provides unprecedented expeditious access to a wide range of optically active spiro[pyrroline-pyrazolones] with various electronic properties in high yields with good to excellent enantioselectivities.
| Year | Citations | |
|---|---|---|
Page 1
Page 1