Australian Journal of Chemistry · 1990 · 86 citations · 0 references
Natural SciencesChemistryMedicinal ChemistryNatural Product BiosynthesisOrganic ChemistryHeterocyclic ChemistryOrganic SynthesisAldehydesChiral Intermediate ProductionCyanohydrin FormationKetonesStereocontrolled Library SynthesisStereoselective Aldol ReactionsStereoselectivityStereoselectivity Control
Cyanohydrins, prepared in high optical purity from aryl aldehydes, have been converted into a- hydroxy aldehydes, ß- hydroxy ketones and ß- hydroxy amines without any racemization and frequently with good stereoselectivity for the erythro-diastereoisomer (>90%) at the newly introduced stereogenic centre.