Stereoselective synthesis of hydroxypyrrolidines and hydroxypiperidines by cyclization of γ-oxygenated-α,β-unsaturated sulfones

This publication has 14 references indexed in Scilit:

• Efficient stereoselective access to polyhydroxylated indolizidine compounds based on .gamma.-hydroxy-.alpha.,.beta.-unsaturated sulfones
  The Journal of Organic Chemistry, 1995
• The diastereofacial selectivity in the intramolecular 1,4-conjugate additions generating substituted tetrahydrothiopyrans follows the Cieplak model
  Tetrahedron Letters, 1995
• Pyrrolizidine alkaloids
  Natural Product Reports, 1995
• Indolizidine and quinolizidine alkaloids
  Natural Product Reports, 1995
• Stereoselective approach to optically pure syn 2-amino alcohol derivatives
  Tetrahedron Letters, 1994
• Highly stereoselective 6-exo ring-closure of 5-substituted hept-6-enyl radicals
  Tetrahedron Letters, 1993
• Regiospecific silver[I] promoted, palladium[O]-catalyzed intramolecular addition of aryl iodides to vinyl sulfones.
  Tetrahedron Letters, 1993
• A practical route to (E)-γ-hydroxy-αβ-unsaturated phenyl sulfones
  Tetrahedron, 1990
• Conjugate addition of internal nucleophile to chiral vinyl sulfoxides with stereogenic center at the allylic carbon. “intramolecular” double asymmetric induction
  Tetrahedron Letters, 1988
• Multiply convergent syntheses via conjugate-addition reactions to cycloalkenyl sulfones
  Chemical Reviews, 1986