Publication | Closed Access
Reduction and Reductive Alkylation of α-<u>tert</u>-Butylthio Carbonyl Compounds. An Efficient Method for Stepwise α-Alkylation of Esters, Nitriles and Ketones Via the α-<u>Tert</u>-Butylthio Derivatives
27
Citations
15
References
1973
Year
Reductive AlkylationChemical EngineeringEnantioselective SynthesisDerivativesApplicable MethodEngineeringDerivative (Chemistry)Natural SciencesKetones ViaDiversity-oriented SynthesisStepwise α-AlkylationStepwise α-AlkylattonOrganic ChemistryCatalysisChemistryChemical DerivativeSynthetic ChemistryStepwise Alkylation
Abstract An efficient and generally applicable method for stepwise α-alkylatton of esters, nitriles, and ketones via the α-tert-butylthio derivatives is described. The method involves reductive-protonation and reductive-alkylation of α-alkylthio α,α-bis-alkylated carbonyl compounds which are prepared by stepwise alkylation of the corresponding simple α-alkylthio carbonyl precursors. The reduction is conveniently performed by use of stoichiometric amounts of a dissolving metal, particularly lithium, affording correspondingly the α-mono-and the α,α-bis-alkylated carbonyl compounds in good yields.
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