A new, economical, practical and racemization-free method for the reductive removal of 2-oxazolidinones from N-acyloxazolidinones with sodium borohydride

This publication has 8 references indexed in Scilit:

• Transesterification of N-acyloxazolidinones with alcohol by lanthanum(III) Iodide
  Tetrahedron Letters, 1998
• Asymmetric synthesis of dideazafolate antitumor agents via amidomethylation of nonracemic oxazolidinone imidates. Synthesis of LY309887, a cytotoxic dideazafolate analog related to lometrexol
  Tetrahedron Letters, 1997
• 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis
  Chemical Reviews, 1996
• Enantioselective synthesis of 2-substituted 4-aminobutanoic acid (GABA) analogues via cyanomethylation of chiral enolates
  Journal of the Chemical Society, Perkin Transactions 1, 1996
• Improved Procedure for the Reduction of N-Acyloxazolidinones
  Synthetic Communications, 1990
• Improved Procedure for the Reduction of Esters to Alcohols by Sodium Borohydride
  Synthetic Communications, 1988
• Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivatives
  Journal of the American Chemical Society, 1982
• The Reduction of Esters with Sodium Borohydride¹
  The Journal of Organic Chemistry, 1963