Tetrahedron Letters p. 9043 - 9046 (1995)
Update date:2022-08-02
Topics:
Dawson, Janet R.
Mellor, John M.
Reaction of amides derived from dichloromaleic anhydride and β-aminomethylstyrenes affords unstable Diels Alder adducts, which give via competing processes a number of products including pyrrolidinones by a novel sequence of dehydrochlorination and subsequent ring-opening of a cyclohexadiene.
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