Stereoselective synthesis of a C-glycoside analogue of N-Fmoc-serine β-N-acetylglucosaminide by ramberg–bäcklund rearrangement

This publication has 15 references indexed in Scilit:

• Glycosylation of Nucleocytoplasmic Proteins: Signal Transduction and O-GlcNAc
  Science, 2001
• Synthesis and Growth Inhibitory Properties of Glucosamine-Derived Glycerolipids
  Organic Letters, 2001
• Methods for Anomeric Carbon-Linked and Fused Sugar Amino Acid Synthesis: The Gateway to Artificial Glycopeptides
  Chemical Reviews, 2000
• Facile synthesis of N-Fmoc-serine-S-GlcNAc: a potential molecular probe for the functional study of O-GlcNAc
  Bioorganic & Medicinal Chemistry Letters, 2000
• Asymmetric Strecker Synthesis of C-Glycopeptide
  The Journal of Organic Chemistry, 2000
• Convergent C-Glycolipid Synthesis via the Ramberg−Bäcklund Reaction: Active Antiproliferative Glycolipids
  Organic Letters, 1999
• Diastereoselective Synthesis of C-Glycosylated Amino Acids with Lactams as Peptide Building Blocks
  Angewandte Chemie International Edition in English, 1999
• Benzylic C-glycosides via the Ramberg-Backlund reaction
  Tetrahedron Letters, 1998
• Synthesis of the C-Analog of 2-Acetylamino-2-deoxy-β-d-glucopyranosyl l- and d-Serine
  Synthesis, 1998
• N‐Halocarbamate Salts Lead to More Efficient Catalytic Asymmetric Aminohydroxylation
  Angewandte Chemie International Edition in English, 1996