Enaminones are organic compounds containing both an enamine and a ketone functional group. They can be synthesized through various methods, including the condensation of a primary amine with a β-ketoester or by reacting a β-dicarbonyl compound with a primary amine. Enaminones are versatile intermediates in organic synthesis and can be used to introduce various substituents into molecules.
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3,5-Pyridinedicarboxylic acid, 1,4-dihydro-4-phenyl-, diethyl ester
2-Propen-1-one, 3-(dimethylamino)-1-(2-pyridinyl)-, (Z)-
3-[5'-isoquinolinylamino]cyclohex-2-en-1-one
2(5H)-Furanone, 5,5-dimethyl-4-(phenylamino)-
(3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl)(phenyl)methanone
Glycine, N-(5,5-dimethyl-3-oxo-1-cyclohexen-1-yl)-, methyl ester
1,3-Propanedione, 1,3-diphenyl-2-[phenyl(phenylamino)methylene]-
(2-chloro-3-pyridinyl)<2-(4-morpholinyl)-1-cyclohexen-1-yl>methanone
1-PYRIDIN-2-YLETHAN-1-ONE OXIME
2-cyclohexen-1-one, 3-[(5-methyl-3-isoxazolyl)amino]-
