Abstract
The microwave-accelerated consecutive reaction of electron deficient (hetero)aryl bromides 1, (hetero)aryl propargyl alcohols 2, and enamino carbonyl compounds 6 or 8 furnishes 1-acetyl-2-amino-cyclohexa-1,3-dienes 7 or 6-N,N-dimethyl carbamoyl-cyclohexenones 9, respectively, in good yields in the sense of one-pot coupling-isomerization-enamine addition-aldol condensation sequence.
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