Oxirane rings: studies and applications of a new chemo and regio selective reductive opening of epoxides

This publication has 11 references indexed in Scilit:

• A facile chemo and regioselective reductive opening of 1,2 epoxides via free radical reaction
  Tetrahedron Letters, 1988
• A new enantio and diastereoselective synthesis of 2-azetidinones as useful intermediates of β-lactan antibiotics
  Tetrahedron Letters, 1988
• Studies on asymmetric synthesis of β-hydroxy-δ-lactone inhibitors of HMGCoA reductase 1. A new preparation of the lactone moiety of compactin
  Tetrahedron Letters, 1987
• A highly stereoselective conversion of α,β-epoxy esters to α-hydroxy esters. An efficient route to optically active α-hydroxyesters
  Tetrahedron Letters, 1987
• Synthesis of Both Enantiomers of Phoracantholide I, a Defensive Secretion of the Eucarypt Longicorn, Employing Asymmetric Reduction with Immobilized Baker’s Yeast
  Chemistry Letters, 1987
• Stereochemical control of nature's biosynthetic pathways:A general strategy for the synthesis 0f polypropionate-derived structural units from a single chiral progenitor
  Tetrahedron, 1987
• Synthetically Useful Reactions of Epoxides
  Synthesis, 1984
• The first practical method for asymmetric epoxidation
  Journal of the American Chemical Society, 1980
• A simple stereoselective synthesis of (R)-recifeiolide by adoption of (R)-methyloxirane as a chiral source
  Tetrahedron Letters, 1977
• Synthesis of optically active forms of sulcatol
  Tetrahedron, 1975