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Azo anions in synthesis: α-amino carbanion equivalents from t-butyldiphenyl-methylhydrazones
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1986
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α-Hydrazino Anion EquivalentsEnantioselective SynthesisEngineeringBiochemistryNatural SciencesDiversity-oriented SynthesisOrganic ChemistryCatalysisC-alkylation ProductsChemistryAzo AnionsSynthetic Chemistryα-Amino Carbanion EquivalentsBiomolecular Engineering
α-Amino carbanion equivalents (NH2) and α-hydrazino anion equivalents (NHNH2) are readily accessible from the C-alkylation products of t-butyldiphenylmethylhydrazones; these azoalkanes can be efficiently transformed into amines, hydrazines, and also alkanes under mild reaction conditions.