Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chlorides

Podobne zapisy

• Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chlorides.
  od: Ley, S, i wsp.
  Wydane: (2004)
• Highly diastereoselective lithium enolate aldol reactions of butane-2,3-diacetal desymmetrized glycolic acid and deprotection to enantiopure anti-2,3-dihydroxy esters.
  od: Dixon, D, i wsp.
  Wydane: (2001)
• Highly diastereoselective ketone aldol reactions of butane-2,3-diacetal desymmetrised glycolic acid
  od: Dixon, D, i wsp.
  Wydane: (2002)
• Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
  od: Ley, S, i wsp.
  Wydane: (2005)
• The use of butane diacetals of glycolic acid as precursors for the synthesis of the phytotoxic calmodulin inhibitor herbarumin II
  od: Diez, E, i wsp.
  Wydane: (2003)