Publication | Closed Access
Chiral <i>N</i>,<i>N</i>′-Dioxide Organocatalyzed Asymmetric Electrophilic α-Cyanation of β-Keto Esters and β-Keto Amides
43
Citations
19
References
2016
Year
Chemical EngineeringNovel Organocatalystsβ-Keto EstersEngineeringβ-Keto AmidesHypervalent IodineOrganic ChemistryChemistryChiral NCyanide-transfer ReagentAsymmetric CatalysisEnantioselective SynthesisBiomolecular Engineering
An enantioselective electrophilic α-cyanation of 1-indanone-derived β-keto esters and β-keto amides using a hypervalent iodine as the cyanide-transfer reagent was realized. A chiral N,N'-dioxide was used as the efficient bifunctional organocatalyst in the presence of inorganic base, which gave the corresponding α-cyano dicarbonyl compounds in yields of 50-99% with good enantioselectivities (87-97% ee).
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