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A New Family of Cinchona-Derived Amino Phosphine Precatalysts: Application to the Highly Enantio- and Diastereoselective Silver-Catalyzed Isocyanoacetate Aldol Reaction
248
Citations
35
References
2011
Year
EngineeringCinchona-derived Amino PhosphineOrganic ChemistryHighly Enantio-ChemistryNovel OrganocatalystsOrganometallic CatalysisStereoselective SynthesisBiochemistryDiversity-oriented SynthesisCatalysisNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringNew FamilyNatural SciencesNew ClassEpicinchona AlkaloidsIsocyanoacetate Nucleophiles
A new class of readily accessible chiral amino-phosphine precatalysts derived from 9-amino(9-deoxy) epicinchona alkaloids has been developed. In combination with Ag(I) salts, these amino-phosphines performed as effective cooperative Brønsted base/Lewis acid catalysts in the asymmetric aldol reaction of isocyanoacetate nucleophiles. Under optimal conditions, high diastereoselectivities (up to 98%) and enantioselectivities (up to 98%) were obtained.
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