Oxidative and reductive ring opening of endo-3,4-O-(4-methoxybenzylidene) acetals of 1, 6-anhydro-β-D-galactopyranoses

This publication has 20 references indexed in Scilit:

• Regioselective reductive ring opening of 4-methoxybenzylidene acetals of hexopyranosides. Access to a novel protective group strategy
  Journal of the Chemical Society, Chemical Communications, 1984
• Reductive Ring Openings of Carbohydrate Benzylidene Acetals Using Borane-Trimethylamine and Aluminium Chloride. Regioselectivity and Solvent Dependance
  Journal of Carbohydrate Chemistry, 1983
• Selective allylation of sugar derivatives containing the 1,1,3,3‐tetraisopropyldisiloxane‐1,3‐diyl protective group
  Recueil des Travaux Chimiques des Pays-Bas, 1983
• Advances in Selective Chemical Syntheses of Complex Oligosaccharides
  Angewandte Chemie International Edition in English, 1982
• A regioselective reductive ring opening of 4,6-O-prop-2-enylidene acetals of hexopyranosides
  Journal of the Chemical Society, Perkin Transactions 1, 1982
• Bausteine von Oligosacchariden, XXX. Neue effektive β‐Glycosidsynthese für Mannose‐Glycoside Synthesen von Mannose‐haltigen Oligosacchariden
  European Journal of Inorganic Chemistry, 1981
• Bausteine von Oligosacchariden, XI: Synthese α‐glycosidisch verknüpfter Disaccharide der 2‐Amino‐2‐desoxy‐D‐galactopyranose
  European Journal of Inorganic Chemistry, 1978
• Hydrogenolysis of carbohydrate acetals, ketals, and cyclic orthoesters with lithium aluminium hydride – aluminium trichloride
  Canadian Journal of Chemistry, 1969
• The Composition of “Mixed Hydride” Reagents. A Study of the Schlesinger Reaction
  Journal of the American Chemical Society, 1966
• THE INFLUENCE OF SUBSTITUENTS ON THE EASE AND DIRECTION OF RING OPENING IN THE LiAlH₄–AlCl₃ REDUCTIVE CLEAVAGE OF SUBSTITUTED 1,3-DIOXOLANES
  Canadian Journal of Chemistry, 1964