| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5233182 | Tetrahedron | 2005 | 7 Pages |
Abstract
A theoretical study was carried out at the B3LYP/6-31G(d) level of calculation in order to predict and interpret the exo/endo ratio of adducts obtained by Diels-Alder cycloaddition of N-benzyl imine of methyl glyoxylate to cyclopentadiene. The theoretical predictions are in good agreement with the experimental study based on NMR spectroscopy.
Related Topics
Physical Sciences and Engineering
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Authors
José Enrique RodrÃguez-Borges, Xerardo GarcÃa-Mera, Franco Fernández, V. Hugo C. Lopes, A.L. Magalhães, M. Natália D.S. Cordeiro,