Article ID Journal Published Year Pages File Type
5388464 Chemical Physics Letters 2009 5 Pages PDF
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 S-phenylethylimine of methyl carboxylate to cyclopentadiene.
Related Topics
Physical Sciences and Engineering Chemistry Physical and Theoretical Chemistry
Preview
Stereoselectivity of the aza-Diels-Alder reaction between cyclopentadiene and protonated phenylethylimine derived from glyoxylates. A density functional theory study
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