Copper(II) bromide is found to be an effective catalyst for the imino Diels–Alder reaction between an imine (generated in situ) and an activated alkene in acetonitrile at the ambient temperature. The reaction proceeds smoothly to afford the corresponding adduct as a mixture of chromatographically separable cis‐ and trans‐isomers in moderate to good yields.
No takes yet. Share an insight, caveat, or question.
Semwal et al. (2006) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: