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Direct Catalytic Enantioselective Aza‐Diels–Alder Reactions
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Citations
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References
2005
Year
Aqueous FormaldehydeEngineeringAryl AminesBiochemistryNatural SciencesDiversity-oriented SynthesisCatalytic SynthesisOrganic ChemistryPeptide ScienceCatalysisStereoselective SynthesisChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringUnmodified α
Proline and its derivatives catalyze the asymmetric one-pot three-component aza-Diels–Alder reaction between unmodified α,β-unsaturated cyclic ketones, aqueous formaldehyde, and aryl amines with excellent chemo- and enantioselectivities (see scheme). Furthermore, this reaction provides a highly enantioselective entry to bicyclic non-proteogenic amino acid derivatives.
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