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Synthesis of 1,6‐dihydro‐5‐hydroxy‐6‐oxo‐3‐(trifluoromethyl)‐4‐pyridazinecarboxylates
32
Citations
4
References
1993
Year
Alkylamine Salts 3A‐gChemical EngineeringAryl HydrazinesN Nmr TechniquesEngineeringOrganic ChemistryChemistryHeterocycle ChemistrySynthetic Chemistry
Abstract The reaction of 2‐(alkylamino)‐3‐(trifluoroacetyl)butenedioates 2a‐b with alkyl and aryl hydrazines in ether provides 1,6‐dihydro‐6‐oxo‐3‐(trifluoromethyl)‐4‐pyridazinecarboxylates as their alkylamine salts 3a‐g . The structures of these products are substantiated using 2D nmr and 15 N nmr techniques.
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