Ring-opening of isoxazolidine nucleus: Competitive formation of α,β-enones and tetrahydro-1,3-oxazines

This publication has 16 references indexed in Scilit:

• Stereoselective synthesis of fused γ-lactams by intramolecular nitrone cycloaddition
  Tetrahedron, 1994
• Stereoselective control in 1,3-dipolar cycloaddition of nitrones to substituted styrenes
  Tetrahedron, 1994
• Ring-opening of isoxazolidine system: Homologation of 3-aryl into 3-styryl nitrones via intermediate 5-hydroxy-isoxazolidines.
  Tetrahedron, 1992
• Novel approach to the ring-opening of 4-isoxazolines: One-pot synthesis of α,β-enones
  Tetrahedron, 1992
• Determination of the stereochemistry of isoxazolidinium salts by nuclear Overhauser effect difference spectroscopy
  Magnetic Resonance in Chemistry, 1988
• Peracid oxidation of 4-isoxazolines as a method for the preparation of .alpha.,.beta.-unsaturated carbonyl compounds
  The Journal of Organic Chemistry, 1988
• The α,α′-dialkylation of cyclic amines. The synthesis of ant venoms.
  Tetrahedron Letters, 1986
• N,O-heterocyclics13;-14conversion of isoxazolidines into α,β enones
  Tetrahedron, 1984
• N,0-heterocyclics-12
  Tetrahedron, 1983
• THE INTRAMOLECULAR NITRONE‐OLEFIN REACTION AND ITS UTILITY IN SYNTHESES OF ALICYCLIC COMPOUNDS*†
  Transactions of the New York Academy of Sciences, 1965