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hello I need the full mechanisms please . CORE MECHANISMS 1,3-Dicarbonyls several synthesis use 1,3-dicarbonyls Hantzsch synthesis Necessarily symmetrical 101HNO but also CAN, MnO2, Cu(NO3)2 R1 Ra COR R2 aldol condensation Michael by enamine enamine-carbonyl cyclocondensation Me CO2Et Write down the starting materials and articulate a mechanism RedoxCORE MECHANISM Enamine formation Michael using enamine Michael using dicarbonyl enamine formation Ra R2 R2 R1R R2 two possible mechanisms R3 ROC COR R2 R2NH3 intramolecular aldol product competes NH2OH only via N-hydroxy dihydropyridine Redox он 32 CHEM3041

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