Stereoselective epoxidation of chiral electron-poor γ-aminoolefins

This publication has 21 references indexed in Scilit:

• 1,4-addition to α,β-unsaturated carbonyl compounds bearing a γ-stereocenter: A molecular mechanics model for steric interactions in the transition state.
  Tetrahedron: Asymmetry, 1990
• Reagent control in the aldol addition of chiral boron enolates based on the 2,5-diphenylborolane ligand system
  Tetrahedron Letters, 1990
• Stereoselective Synthesis of γ‐Aminocarboxylates
  Angewandte Chemie International Edition in English, 1989
• Stereoselektive Synthese von γ‐Aminocarbonsäureestern
  Angewandte Chemie, 1989
• Protective group tuning in the stereoselective conversion of α-amino aldehydes into aminoalkyl epoxides
  Tetrahedron Letters, 1989
• A simple synthetic route to statine and statine analogues
  Journal of the Chemical Society, Chemical Communications, 1989
• Asymmetric C-C bond formation using organometallic chemistry
  Published by Walter de Gruyter GmbH ,1988
• Stereoselective Synthesis of β‐Amino Alcohols from Optically Active α‐Amino Acids
  Angewandte Chemie International Edition in English, 1987
• Stereoselektive Synthese von β‐Aminoalkoholen aus optisch aktiven α‐Aminosäuren
  Angewandte Chemie, 1987
• Lanthanides in organic synthesis. 4. Reduction of .alpha.,.beta.-epoxy ketones with samarium diiodide. A route to chiral, nonracemic aldols
  The Journal of Organic Chemistry, 1986