Synthesis of C-glycosyl compounds by the wittig iodocyclization procedure. Differences from mercuriocyclization

This publication has 18 references indexed in Scilit:

• Stereoselectivity in the electrophile-promoted cyclizations of a hydroxyolefin derived from arabinose. Synthesis of a phosphonate isostere of β-(=D)-arabinose-1, 5-diphosphate
  Tetrahedron Letters, 1985
• High stereoselective synthesis of diethyl (2,3-isopropylidene-5-trityl-α-d-ribofuranosyl)-methanephosphonate, a precursor to the phosphono analog of α-d-ribose 1-phosphate
  Tetrahedron Letters, 1984
• Synthesis of the phosphono analogues of α- and β-d-mannopyranosyl phosphate
  Carbohydrate Research, 1984
• Formation of convenient chiral intermediates from carbohydrates and their use in synthesis
  Tetrahedron, 1984
• C-glycosides through the Wittig-cyclization procedure: Observations on the influence of the nature of the substrate.
  Tetrahedron Letters, 1984
• Stereospecific synthesis of the phosphono analogs of .alpha.- and .beta.-D-glucose 1-phosphate
  The Journal of Organic Chemistry, 1982
• Synthesis of the phosphono-analogue of α-D-glucose 1-phosphate
  Journal of the Chemical Society, Chemical Communications, 1982
• Synthesis of phosphonate analogs of α-d-glucopyranosyl and α-d-galactopyranosyl phosphate
  Carbohydrate Research, 1981
• Synthesis of Naturally Occurring C-Nucleosides, Their Analogs, and Functionalized C-Glycosyl Precursors
  Published by Elsevier ,1976
• C-Glycosyl nucleosides. V. Unexpected observations on the relative stabilities of compounds containing fused five-membered rings with epimerizable substituents
  Journal of the American Chemical Society, 1975