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2,3-Dihydro-4-pyridone skeleton is an important building block in organic synthesis because it features several reaction sites with nucleophilic or electrophilic properties. Herein, we disclose a method for its formation by intramolecular cyclization of ester-tethered enaminones, which can easily be synthesized from readily available materials, such as
Milovan Stojanović +2 more
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ChemInform Abstract: ACYLATION OF 4‐PYRIDONE
Chemischer Informationsdienst, 1980AbstractBei der Acylierung von 4‐Pyridon (I) mit aliphatischen Carbonsäure‐anhydriden und ‐chloriden oder freien Säuren in Gegenwart von Dicyclohexylcarbodiimid erhält man ausschließlich die N‐Acyl‐4‐pyridone (III).
F. EFFENBERGER, A. O. + MUECK, E. BESSEY
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Synthesis of Some N-dialkylaminoalkyl-4-pyridones
Journal of the American Pharmaceutical Association (Scientific ed.), 1950Attempts to prepare some N-dialkylaminoalkyl-4-alkoxy- and 4-aryloxy-2-pyridones by oxidation of N-dialkylaminoalkyl-4-alkoxy- and 4-aryloxy-pyridinium halides with potassium ferricyanide in alkaline solution resulted instead in the formation of N-dialkylaminoalkyl-4-pyridones as a result of cleavage of the 4-alkoxy or 4-aryloxy group under the ...
J H, SHINKAI, L M, PARKS
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Synthetic Applications of Chiral 2,3‐Dihydro‐4‐pyridones
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Sajan, Joseph, Daniel L, Comins
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