Stereoselective alkylation of chiral glycine enolate synthons. The enantioselective synthesis of α-amino acid derivatives.

This publication has 12 references indexed in Scilit:

• Asymmetric synthesis of α-amino acids by alkylation of a glycine amide derivative bearing chiral 2,5-disubstituted pyrrolidine as an amine component
  Tetrahedron Letters, 1986
• The Facile and Efficient Preparation of Phenolic and Thiol Esters
  Synthetic Communications, 1986
• Electrophilic glycinates: new and versatile templates for asymmetric amino acid synthesis
  Journal of the American Chemical Society, 1986
• Influence of pseudoallylic strain on the conformational preference of 4-methyl-4-phenylpipecolic acid derivatives
  The Journal of Organic Chemistry, 1985
• Asymmetric Synthesis of Alanine by Alkylation of Optically Active N-Alkyl-N-formylaminoacetonitriles
  Bulletin of the Chemical Society of Japan, 1978
• Synthesis of 2,6-diacetonylpiperidine. X-ray diffraction analysis of its N-benzoyl derivative
  The Journal of Organic Chemistry, 1978
• Reduction of amino acids to amino alcohols. A comparison of various methods with regard to potential racemization
  Tetrahedron Letters, 1977
• Sterically controlled syntheses of optically active organic compounds. XV. Synthesis of optically active aspartic acid through .beta.-lactam
  The Journal of Organic Chemistry, 1972
• .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines
  The Journal of Organic Chemistry, 1969
• Allylic strain in six-membered rings
  Chemical Reviews, 1968