Solid‐Phase Synthesis of a Phytoalexin Elicitor Pentasaccharide Using a 4‐Azido‐3‐chlorobenzyl Group as the Key for Temporary Protection and Catch‐and‐Release Purification

This publication has 30 references indexed in Scilit:

• Solid-Phase Synthesis of a Phytoalexin Elicitor-Active Tetraglucosyl Glucitol
  Synlett, 2002
• A New Catch-and-Release Purification Method Using a 4-Azido-3-chlorobenzyl Group
  Synlett, 2001
• Automated Solid-Phase Synthesis of Oligosaccharides
  Science, 2001
• Solid Phase Syntheses of Oligomannosides and of a Lactosamine Containing Milk Trisaccharide Using a Benzoate Linker
  Synthesis, 2001
• A Novel Oxidatively Removable Linker and Its Application to α-Selective Solid-Phase Oligosaccharide Snythesis on a Macroporous Polystyrene Support
  Synlett, 1999
• Investigating highly crosslinked macroporous resins for solid-phase synthesis
  Bioorganic & Medicinal Chemistry Letters, 1998
• 4-Azido-3-chlorobenzyl Ether, New Protection for Hydroxy Functions
  Synlett, 1997
• 1,6-Anhydro-β-D-glucopyranose derivatives as glycosyl donors for thioglycosidation reactions
  Journal of the Chemical Society, Perkin Transactions 1, 1990
• A new synthetic route to tert-butyloxycarbonylaminoacyl-4-(oxymethyl)phenylacetamidomethyl-resin, an improved support for solid-phase peptide synthesis
  The Journal of Organic Chemistry, 1978
• The monitoring of reactions in solid-phase peptide synthesis with picric acid
  Analytica Chimica Acta, 1972