Publication | Closed Access
Concise Synthesis of Novel Practical Sulfamide−Amine Alcohols for the Enantioselective Addition of Diethylzinc to Aldehydes
57
Citations
14
References
2004
Year
Grafting StrategyConcise SynthesisMedicinal ChemistryCombinatorial ChemistryAsymmetric AdditionBiochemistryNatural SciencesOrganic ChemistryOrganometallic CatalysisEnantioselective AdditionStereoselective SynthesisChemistryAbsolute Configuration ProductsAsymmetric CatalysisSynthetic ChemistryEnantioselective Synthesis
Novel sulfamide-amine alcohol ligands were designed using a grafting strategy and synthesized from readily available starting materials via a simple, efficient method. The key features of these ligands for the asymmetric addition of diethylzinc to aldehydes included stability, enhanced effectiveness without using Ti(O(i)Pr)(4), suitability for a variety of aldehydes, the ability to operate at room temperature, and selectability to afford either absolute configuration products with enantiomeric excess up to >99%.
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