Abstract
The reaction of α-diketones
with malononitrile has been shown to give either
simple Knoevenagel adducts or substituted γ-lactams,
depending on the proportions of the reactants used. The behaviour of the adduct
(la) towards nucleophilic attack has been investigated and the resulting
reactions rationalized. The published structures of the products from the
reactions of malononitrile dimer with benzil and from
malononitrile with benzoin have been reassigned.
Cited by
22 articles.
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