Highly Regioselective Lewis Acid-Mediated Aldol Additions at the More Encumbered α-Side of Unsymmetrical Ketones

This publication has 11 references indexed in Scilit:

• Alkali Enolates of Unsymmetrical Ketones from Silyl Enol Ethers. Highly Regioselective Aldol Reactions Dependent on the Nature of the Cation
  The Journal of Organic Chemistry, 1996
• Catalytic, Diastereoselective Aldol Reactions Using Titanium(IV) Halides
  European Journal of Inorganic Chemistry, 1995
• A New Stereoselective Aldol Reaction using α-(Phenylseleno)Cycloalkanones
  Phosphorus, Sulfur, and Silicon and the Related Elements, 1992
• Simple diastereoselectivity of the aldol reaction of persubstituted enolates. Stereoselective construction of quaternary centers
  The Journal of Organic Chemistry, 1991
• The [18] all-carbon molecule: cumulene or polyacetylene?
  Journal of the American Chemical Society, 1991
• Preparation of a new, highly reactive form of iron(0), and its use in deprotonation of carbonyl compounds
  The Journal of Organic Chemistry, 1984
• Tris(dialkylamino)sulfonium enolates. Synthesis, structure, and reactions
  Journal of the American Chemical Society, 1983
• Selective carbon-carbon bond formation via transition metal catalysis. 29. A highly regio- and stereospecific palladium-catalyzed allylation of enolates derived from ketones
  The Journal of Organic Chemistry, 1982
• New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride
  Journal of the American Chemical Society, 1974
• Chemistry of carbanions. XXIII. Use of metal complexes to control the aldol condensation
  Journal of the American Chemical Society, 1973