THE RING CONTRACTION OF DELTA-LACTONES WITH LEAVING GROUP ALPHA-SUBSTITUENTS - A STRATEGY FOR THE SYNTHESIS OF 2,5-DISUBSTITUTED HIGHLY FUNCTIONALIZED HOMOCHIRAL TETRAHYDROFURANS

Podobne zapisy

• ACID-CATALYZED TRANSFORMATION OF ALPHA-TRIFLUOROMETHANESULFONATES OF GAMMA-LACTONES AND DELTA-LACTONES INTO 2,5-DISUBSTITUTED HOMOCHIRAL TETRAHYDROFURANS
  od: Wheatley, J, i wsp.
  Wydane: (1993)
• CYCLIC SULFATES OF DELTA-LACTONES IN THE SYNTHESIS OF TETRAHYDROFURANS TETRAHYDROPYRANS AND CYCLOHEXANES
  od: Skead, B, i wsp.
  Wydane: (1993)
• Branched tetrahydrofuran alpha,alpha-disubstituted-delta-sugar amino acid scaffolds from branched sugar lactones: a new family of foldamers?
  od: Simone, M, i wsp.
  Wydane: (2005)
• Complex tetrahydrofurans from carbohydrate lactones: Easy access to epimeric C-glycosides of glucofuranose from D-glycero-D-gulo-heptono-1,4-lactone
  od: Bichard, C, i wsp.
  Wydane: (1996)
• Templated scaffolds of cis- and trans-tetrahydrofuran gamma-amino acids: gamma-azido-beta-hydroxy-tetrahydrofuran-2-carboxylates from pentono-delta-lactones
  od: Sanjayan, G, i wsp.
  Wydane: (2003)