Abstract
Structures are proven for the products of Michael addition of malonate esters to methyl and ethyl trans-benzylisatylideneacetate. There are described the reactions of the pyrrolidine enamine of cyclopentanone with cinnamaldehyde and ethyl cinnamate to give the expected Stork condensation products, and its reaction with ethyl benzylisatylideneacetate to give unexpected products.
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