Lanthanide trifluoromethanesulfonates as reusable catalysts. Michael and Diels-Alder reactions

This publication has 25 references indexed in Scilit:

• Application of lanthanide reagents in organic synthesis
  Chemical Reviews, 1992
• [1,2-Benzenediolato(2−)-O,O′]oxotitanium. A Mild and Efficient Catalyst for the Michael Reaction of Ketene Silyl Acetals with α,β-Unsaturated Ketones
  Chemistry Letters, 1989
• The Michael Reaction of O-Silylated Ketene Acetals with α,β-Unsaturated Esters Promoted by a Catalytic Amount of Aluminum Triflate
  Chemistry Letters, 1987
• A Significant Substituent Effect on the Stereochemistry of the Trityl Salt-Catalyzed Michael Reaction
  Chemistry Letters, 1987
• An Efficient and Extremely Mild Catalyst System, Combined Use of Trityl Chloride and Tin(II) Chloride, in the Aldol and Michael Reactions
  Chemistry Letters, 1987
• An Essentially Mild and Efficient Catalyst System for the Activation of Carbonyl Compounds and Their Derivatives. The Combined Use of Trimethylsilyl Chloride and Tin(II) Chloride
  Chemistry Letters, 1987
• Totally Synthetic Routes to the Higher Monosaccharides
  Angewandte Chemie International Edition, 1987
• Clay montmorillonite-catalysed Michael reactions of silyl ketene acetals and a silyl enol ether with α,β-unsaturated carbonyl compounds
  Journal of the Chemical Society, Chemical Communications, 1987
• THE STEREOSELECTIVE MICHAEL REACTION BETWEEN SILYL ENOL ETHERS AND α,β-UNSATURATED KETONES BY THE USE OF TRITYL PERCHLORATE AS A CATALYST
  Chemistry Letters, 1986
• THE TRITYL PERCHLORATE CATALYZED MICHAEL REACTION
  Chemistry Letters, 1985