Publication | Open Access
Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers through Copper‐Catalyzed Conjugate Additions of Aryl‐ and Alkylaluminum Reagents to Acyclic Trisubstituted Enones
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Citations
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References
2013
Year
Asymmetric CatalysisChemical EngineeringNovel OrganocatalystsAlkylaluminum ReagentsEngineeringAcyclic Quaternary CarbonsOrganic ChemistryAvailable OrganolithiumsOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryConjugate AdditionAcyclic Trisubstituted EnonesEnantioselective SynthesisBiomolecular Engineering
Acyclic quaternary carbons by conjugate addition: The first examples of catalytic enantioselective conjugate additions of aryl and alkyl units that generate acyclic all-carbon quaternary stereogenic centers have been developed (see scheme). The requisite organoaluminum reagents can either be prepared in situ from easily available organolithiums or purchased at low cost.
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