Glycosyl .alpha.-amino acids via stereocontrolled buildup of a penaldic acid equivalent. A novel synthetic approach to the nucleosidic component of the polyoxins and related substances

This publication has 11 references indexed in Scilit:

• Synthesis of D‐Erythro‐ and D‐Threo‐Sphingosine Derivatives From L‐Serine
  Helvetica Chimica Acta, 1988
• The synthesis and configurational stability of differentially protected .beta.-hydroxy-.alpha.-amino aldehydes
  The Journal of Organic Chemistry, 1987
• Rapid and convenient syntheses of polyoxin peptides containing N-methylated peptide bonds
  The Journal of Organic Chemistry, 1986
• Total synthesis of optically active N-benzoyldaunosamine from an azetidinone
  The Journal of Organic Chemistry, 1984
• Chiral transformations of D-ribose to 2(S)-amino-2-[2,5-dihydro-5(R)-methylfuran-2(R)-yl]ethanoic acid, a diastereomer of the antibiotic (+)-furanomycin
  Canadian Journal of Chemistry, 1983
• Chiral transformations of D-ribose to 2-(β-D-ribofuranosyl)-L and D-glycine and an anhydroallose hemiacetal used in C-nucleoside synthesis
  Canadian Journal of Chemistry, 1983
• Totalsynthese von Nojirimycin
  Helvetica Chimica Acta, 1982
• Nucleoside syntheses, XXII¹⁾Nucleoside synthesis with trimethylsilyl triflate and perchlorate as catalysts
  European Journal of Inorganic Chemistry, 1981
• Total synthesis of (+)-furanomycin and stereoisomers
  Journal of the American Chemical Society, 1980
• The Synthesis of Triazole Analogs of Histamine and Related Compounds
  Journal of the American Chemical Society, 1949