Efficient method for introducing vineomycin-fridamycin-type side chain. Total synthesis of fridamycin E

This publication has 12 references indexed in Scilit:

• Preparation of enantiomerically enriched compound using enzymes. Part 3. Enzymic preparation of enantiomerically enriched tertiary .alpha.-benzyloxy acid esters. Application to the synthesis of (S)-(-)-frontalin
  The Journal of Organic Chemistry, 1990
• Synthetic study toward vineomycins. Synthesis of c-aryl glycoside sector via Cp2HfCl2AgClO4-promoted tactics
  Tetrahedron Letters, 1989
• Synthesis of - and -fridamycin E
  Tetrahedron, 1988
• New approach to C-aryl glycosides starting from phenol and glycosyl fluoride. Lewis acid-catalyzed rearrangement of O-glycoside to C-glycoside
  Tetrahedron Letters, 1988
• Superbases for organic synthesis
  Published by Walter de Gruyter GmbH ,1988
• On the selectivity of deprotection of benzyl, mpm (4-methoxybenzyl) and dmpm (3,4-dimethoxybenzyl) protecting groups for hydroxy functions
  Tetrahedron, 1986
• The structure of vineomycin B2.
  The Journal of Antibiotics, 1981
• New antitumor antibiotics, OS-4742 A1, A2, B1 and B2 produced by a strain of Streptomyces.
  The Journal of Antibiotics, 1977
• Zur aktivierung lithiumorganischer reagenzien
  Journal of Organometallic Chemistry, 1967
• On the interaction of organolithium compounds with sodium and potassium alkoxides. A new method for the synthesis of organosodium and organopotassium compounds
  Tetrahedron Letters, 1966