Further Study toward Amipurimycin: Synthesis of the Northern Part

This publication has 12 references indexed in Scilit:

• Chain Extension of Carbohydrates VI. Synthesis of the Two C-6 Epimers of the 6-Acetylamino-4,6-dideoxyheptopyranosiduronic Acid Present in Amipurimycin by Means of Stereocontrolled Ethynylation of Methyl 2,3-Di-O-benzyl-4-deoxy-α-d-xylo-hexodialdo-1,5-pyranoside
  Bulletin of the Chemical Society of Japan, 1996
• Deoxygenation at C-4 and Stereospecific Branched-Chain Construction at C-3 of a Methyl Hexopyranuloside. Synthetic Approach to the Amipurimycin Sugar Moiety
  The Journal of Organic Chemistry, 1996
• Synthesis of Complex Nucleoside Antibiotics
  Chemical Reviews, 1995
• Nucleophilic Substitution Versus Radical Reaction for Carbohydrates Deoxygenation: Application at c-4 of Methyl-α-D-Glucopyranoside Derivatives
  Journal of Carbohydrate Chemistry, 1995
• A glycosylation reaction: Conversion of methyl glicosides to glycosyl chlorides by boron trichloride
  Tetrahedron Letters, 1987
• Structure of amipurimycin, a nucleoside antibiotic having a novel branched sugar moiety
  Tetrahedron Letters, 1982
• 2-Methylthio-7-desazainosin und sein α-Anomer — Debenzylierung von Thionucleosiden mit Bortrichlorid
  European Journal of Organic Chemistry, 1982
• A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compounds
  The Journal of Organic Chemistry, 1981
• Isolation and characterization of a new nucleoside antibiotic, amipurimycin.
  The Journal of Antibiotics, 1977
• Streptomyces novoguineensis sp. nov., an amipurimycin producer, and antimicrobial activity of amipurimycin.
  The Journal of Antibiotics, 1977