Summary of properties of compounds 32 to 37.

Compound	Condition of synthesis	Yield (%)	Activity	Outcome	Reference
32–35	32 and 34: 6–8 h reflux of α,β-unsaturated carbonyl compounds with NH2OH·HCl in EtOH	42–62	Anticancer	34f and 34g were the most potent anticancer agents	60
	33 and 35: 8 h reflux of 32 and 34 with haloalkylamine in dry acetone in presence of K2CO3
36a–h	Reflux of α,β-unsaturated carbonyl compounds with NH2OH·HCl in EtOH	39–51	Anticancer	36g and 36h were the most potent anticancer agents	61
37a–k	Stirring of precursors for 5 h at 0–5 °C in dry acetone in presence of K2CO3	48.2–76	Anti-inflammatory	37j was the most potent anti-inflammatory agent	62