NEW STRATEGY FOR THE SYNTHESIS OF THE TAXANE DITERPENES - FORMATION OF THE 8-MEMBERED B-RING OF TAXOL BY SEMI-PINACOL REARRANGEMENT

Podobne zapisy

• Taxane diterpenes .3. Formation of the eight-membered B-ring by semi-pinacol rearrangement
  od: Magnus, P, i wsp.
  Wydane: (1996)
• NEW STRATEGY FOR THE SYNTHESIS OF THE TAXANE DITERPENES - FORMATION OF THE BC-RINGS OF TAXOL VIA A [5+2]-PYRYLIUM YLIDE-ALKENE CYCLIZATION, RING EXPANSION STRATEGY
  od: Bauta, W, i wsp.
  Wydane: (1995)
• Taxane diterpenes .2. Synthesis of the 7-deoxy ABC taxane skeleton, and reactions of the A-ring
  od: Magnus, P, i wsp.
  Wydane: (1996)
• Taxane diterpenes .1. Control of relative and absolute stereochemistry in intramolecular pyrylium ylide-alkene cyclizations for the synthesis of taxol precursors.
  od: Bauta, W, i wsp.
  Wydane: (1996)
• Brönsted Acid of Keggin Type Polyoxometalate Catalyzed Pinacol Rearrangement
  od: Aldes Lesbani, i wsp.
  Wydane: (2014-08-01)