STEREOSELECTIVE SYNTHESIS OF ERYTHRO-BETA-HYDROXY CARBOXYLIC-ACIDS VIA IRON ACYL COMPLEXES

Podobne zapisy

• CHIRAL PROPIONATE ENOLATE EQUIVALENTS FOR THE STEREOSELECTIVE SYNTHESIS OF THREO-ALPHA-METHYL-BETA-HYDROXY OR ERYTHRO-ALPHA-METHYL-BETA-HYDROXY ACIDS
  od: Davies, S, i wsp.
  Wydane: (1985)
• STEREOSELECTIVE PREPARATION OF BETA-AMINO-ACYL IRON COMPLEXES FOR BETA-LACTAM SYNTHESIS
  od: Broadley, K, i wsp.
  Wydane: (1984)
• CHIRAL ACETATE ENOLATE EQUIVALENT FOR THE SYNTHESIS OF BETA-HYDROXY ACIDS
  od: Davies, S, i wsp.
  Wydane: (1984)
• Asymmetric synthesis of beta-lactams and pseudopeptides via stereoselective conjugate additions of lithium (alpha-methylbenzyl)-allylamide to alpha,beta-unsaturated iron acyl complexes
  od: Davies, S, i wsp.
  Wydane: (1999)
• Asymmetric synthesis via iron acyl complexes
  od: Walker, J, i wsp.
  Wydane: (1986)