The role of hard Lewis acids in the tunning of the exo/endo stereoselectivity in Diels-Alder reactions: ab initio calculations
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry
Reference22 articles.
1. Mechanistic Aspects of Diels-Alder Reactions: A Critical Survey
2. Einfluss von lewis-säuren auf das endo-exo-verhaltnis bei diels-alder-additionen des cyclopentadiens
3. Catalytic Actions of Aluminum Chloride on the Isoprene—Methyl Acrylate Diels-Alder Reaction
4. Aluminum Chloride Catalyzed Diene Condensation. II.1 Stronger Adherence to the Alder endo Rule
5. Endo selectivities of some methyl-substituted dienophiles in Diels-Alder reactions with cyclopentadiene
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1. A DFT Study of the Molecular Mechanisms of the Diels−Alder Reaction between Cyclopentadiene and 3-Phenyl-1-(2-pyridyl)-2-propen-1-one − Role of the Zn2+ Lewis Acid Catalyst and Water Solvent;European Journal of Organic Chemistry;2002-08
2. Density functional theory study of the Lewis acid-catalyzed Diels-Alder reaction of nitroalkenes with vinyl ethers using aluminum derivatives;Journal of Physical Organic Chemistry;2002
3. Computational Studies on the BF3-Catalyzed Cycloaddition of Furan with Methyl Vinyl Ketone: A New Look at Lewis Acid Catalysis;The Journal of Organic Chemistry;2000-09-01
4. Theoretical Study of 1,3-Dipolar Cycloaddition Reactions with Inverse Electron Demand − A DFT Study of the Lewis Acid Catalyst and Solvent Effects in the Reaction of Nitrones with Vinyl Ethers;European Journal of Organic Chemistry;2000-06
5. A Three-Center Orbital Interaction in the Diels−Alder Reactions Catalyzed by Lewis Acids;The Journal of Organic Chemistry;2000-03-01
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