The “cieplak effect”: Hyperconjugative interactions in diels alder reactions.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Heteroatom-directed .pi.-facial diastereoselection in Diels-Alder cycloadditions of plane-nonsymmetric cyclopentadienes
2. π-Facial diastereoselectivity in Diels-Alder reactions of 2,5-dimethylthiophene oxide
3. Reversal of .pi.-facial diastereoselection upon electronegative substitution of the substrate and the reagent
4. A theoretical study of tautomerism in the gas phase and aqueous solution: a combined use of state-of-the-art ab initio quantum mechanics and free energy-perturbation methods
5. Hyperconjugation as a factor in face selectivity during cycloaddition
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