Synthesis · 2005 · 23 citations · 0 references
Natural SciencesChemistryOrganic ChemistryOrganometallic ChemistrySynthetic Medicinal ChemistryAmino Acid ChemistryOrganic SynthesisAlkylation ProcessesAlkylation ReactionsAmination ReactionsAmino Acid DerivativesAmino Acid Esters
An efficient, general procedure for reductive monoalkylation of amines and amine derivatives with aldehydes is reported. Treatment of aldehydes with primary amines, secondary amines, O-trimethylsilylhydroxylamine, and N,N-dimethylhydrazine in lithium perchlorate/diethyl ether and trimethylsilyl chloride, followed by BH3·NEt3 reduction, and straightforward workup afforded secondary amines, tertiary amines, N-substituted hydroxylamines, and hydrazines, respectively. Reductive alkylation of α-amino esters with aldehydes afforded the corresponding N-monoalkylated α-amino esters selectively.