125732-50-5Relevant articles and documents
MICHAEL-TYPE ADDITION REACTIONS OF SOME ENAMINES TO ARYLIDENEPYRAZOLONES
Abdel-Rahman, M.,Abdel-Ghany, H.
, p. 1987 - 1996 (2007/10/02)
The reaction of the arylidenepyrazolones (1b-d) with 1-morpholinocyclohexene (E2) in refluxing acetonitrile leads to the less substituted alkylated enamines 3b-d.On the other hand, the more substituted alkylated enamines 2a-d are formed when 1a-d react under the same conditions with 1-piperidinocyclohexene (E1).The nature of the enamine in crucial.Nucleophilic attack of the enamine on the α,β-unsaturated carbonyl system of 1 gives rise to a zwitterionic intermediate which through α-proton loss leads to different Michael-type adducts depending on the enamine.