The Michael addition is a well-known reaction in organic chemistry where a nucleophile (a species with a pair of electrons to donate) adds to a π-unsaturated system, often an α,β-unsaturated carbonyl compound. When this reaction involves a nitrogen atom (aza-Michael), it typically results in the formation of a new carbon-nitrogen bond. In this context, the intramolecular aza-Michael addition means that the reaction takes place within the same molecule.
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N-benzyloxycarbonyl-(E)-4-(2-aminophenyl)-1-phenylbut-2-en-1-one
N-{2-[3-(3,4-dimethoxyphenyl)acryloyl]phenyl}acetamide
(2'S)-5-bromo-1-[1'-(tert-butyldiphenylsilyloxy)-4'-hydroxybutan-2'-yl]-4-chloro-1H-pyrrole-2-carbonitrile
4(1H)-Quinolinone, 2,3-dihydro-2-phenyl-1-(phenylsulfonyl)-
