Publication | Closed Access
Cinchona alkaloid thiourea mediated asymmetric Mannich reaction of isocyanoacetates with isatin-derived ketimines and subsequent cyclization: enantioselective synthesis of spirooxindole imidazolines
42
Citations
77
References
2015
Year
High YieldsAsymmetric Mannich ReactionNovel OrganocatalystsEngineeringBiochemistryExcellent StereoselectivitiesNatural SciencesIsatin KetiminesOrganic ChemistryCinchona Alkaloid ThioureaStereoselective SynthesisChemistrySpirooxindole ImidazolinesPharmacologyAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringNatural Product Synthesis
The organocatalyzed asymmetric Mannich reaction of isocyanoacetates with isatin ketimines and subsequent cyclization were developed, leading to spirooxindole imidazolines in high yields and excellent stereoselectivities.
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