Synthetic Communications · 2000 · 17 citations · 3 references
Natural SciencesChemistryOrganic ChemistryChemical ReductionHeterocyclic ChemistryOrganic SynthesisOxidation-reduction ReactionsAroma Compound ReductionAsymmetric ReductionsAsymmetric SynthesisChiral Product SynthesisEnantioselective ReductionImine ReductionOrganic Reduction Reactions
Abstract Zirconium borohydride, a potential reducing agent, reduces acids, esters, imines to the corresponding alcohols and secondary amines in good yield at room temperature within two hours. This facile reducing property was taken advantage off in the synthesis of pheromones and some novel chiral precursors for asymmetric synthesis.
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Herbert C. Brown, Yong M. Choi, S. Narasimhan · The Journal of Organic Chemistry · 1982 · 139 citations
REDUCTION OF a-AMINO ACIDS: L-VALINOL
Organic Syntheses · 1985 · 18 citations