Branched-chain Sugars. XXIII. Stereoselectivities in the Addition of Nucleophiles to Several 4-Uloses

This publication has 15 references indexed in Scilit:

• Branched-chain Sugars. XIX. On the Application of 13C NMR Spectroscopy to the Configurational Assignment of 3-C-Substituents of Aldohexopyranose Derivatives
  Bulletin of the Chemical Society of Japan, 1980
• The orthosomycin family of antibiotics—I
  Tetrahedron, 1979
• Synthesis of methyl 4-amino-4,6-dideoxy-α-d-galactopyranoside from a glycosulose precursor
  Carbohydrate Research, 1978
• Assignment of configuration at quaternary centres in pairs of 3-C Hydroxymethyl and 3-C methyl branched chain 1,2:4,6-diacetalated aldohexopyranose derivatives using 13C-N.M.R. spectoscopy
  Carbohydrate Research, 1978
• Verzweigte Zucker, XXII: Synthese der Isomeren der hydroxyethyl‐verzweigten γ‐Octose
  European Journal of Inorganic Chemistry, 1978
• Monomolar acetalations of methyl α-d-mannosides—synthesis of methyl α-d-talopyranoside
  Carbohydrate Research, 1977
• Carbon-13 nuclear magnetic resonance spectra of branched-chain sugars. Configurational assignment of the branching carbon atom of methyl branched-chain sugars
  The Journal of Organic Chemistry, 1974
• Synthesis of macrolide antibiotics. I. Stereospecific addition of methyllithium and methylmagnesium iodide to methyl .alpha.-D-xylo-hexopyranosid-4-ulose derivatives. Determination of the configuration at the branching carbon atom by carbon-13 nuclear magnetic resonance spectroscopy
  The Journal of Organic Chemistry, 1974
• The synthesis of methyl 6-deoxy-2,3-O-isopropylidene-α-D-ribo-hexopyranosid-4-ulose
  Carbohydrate Research, 1974
• Application de la RMN du 13C a la determination de la configuration de centres quaternaires en serie alicyclique et hydrate de carbone a chaine ramifiee
  Tetrahedron, 1974