Publication | Closed Access
Asymmetric Formal Carbonyl-Ene Reactions of Formaldehyde <i>tert</i>-Butyl Hydrazone with α-Keto Esters: Dual Activation by Bis-urea Catalysts
90
Citations
28
References
2012
Year
EngineeringTertiary CarbinolsOrganic ChemistryChemistryα-Keto EstersChemical EngineeringDiversity Oriented SynthesisOrganometallic CatalysisDiversity-oriented SynthesisBis-urea CatalystsCatalysisNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisCatalytic SynthesisBiomolecular EngineeringNatural SciencesDual ActivationBinam-derived Bis-ureas
The dual activation of α-keto esters and formaldehyde tert-butyl hydrazone by BINAM-derived bis-ureas is the key to achieve high reactivity and excellent enantioselectivities in nucleophilic addition (formal carbonyl-ene reaction) to functionalized tertiary carbinols. Ensuing high-yielding diazene-to-aldehyde tranformations and subsequent derivatizations provides a direct entry to a variety of densely functionalized products.
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