Publication | Open Access
Direct Formation of the Carbonyl Anion of Diisopropyl Formamide
51
Citations
2
References
1974
Year
Direct FormationFormyl ProtonEngineeringBiochemistryNatural SciencesCyanohydrin FormationOrganic ChemistryLithium Diisopropylamide ProducesStereoselective SynthesisChemistryDerivative (Chemistry)Synthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The reaction of diisopropyl formamide with lithium diisopropylamide produces, by abstraction of the formyl proton, the carbonyl anion, LiCON[CH(CH 3 ) 2 ] 2 . Reactions of this anion with benzaldehyde, benzophenone, ethyl benzoate, acetone, and propionaldehyde occur in yields ranging from 30–92%. Thus, this anion provides a useful method for the synthesis of α-hydroxy and α-keto acids, particularly in cases where cyanohydrin formation is difficult.
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