1977
DOI: 10.1055/s-1977-24596
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A Convenient Method for the Preparation of 2-Pyridone Derivatives

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1978
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Cited by 24 publications
(4 citation statements)
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“…5 The new compounds, which to our knowledge have not been described previously, are: 3-cyano-4-( 2-chlorophenyl )-6-phenyl-2(1H)-pyridone, m.p. 268-2708C;3cyano-4-(2,6-bichlorophenyl)-6-phenyl-2(1H)-pyridone, m.p.…”
mentioning
confidence: 78%
“…5 The new compounds, which to our knowledge have not been described previously, are: 3-cyano-4-( 2-chlorophenyl )-6-phenyl-2(1H)-pyridone, m.p. 268-2708C;3cyano-4-(2,6-bichlorophenyl)-6-phenyl-2(1H)-pyridone, m.p.…”
mentioning
confidence: 78%
“…In cases in which it was clear that products were being formed relatively quickly, these were collected a t 2-hourly intervals. The nitrile products (7) did not always crystallise readily, and accordingly in a few cases it was necessary to remove the solvent and recrystallise the residual gum from methanol. The proportions of the products varied according to the substituents and, to some extent, the length of heating.…”
Section: Reaction Of 3-carbamoyl-2-iminochro~~ten Derivat Ives Withmentioning
confidence: 99%
“…In addition, 4,6-diaryl-3-cyano-2-pyridones were prepared by the reaction between 1,3-diaryl-2-propen-1-ones and cyanoacetamide using powdered KOH under microwave irradiation [23]. One of the less explored synthesis of 4-(substituted phenyl)-6-phenyl-3-cyano-2-pyridones is their synthesis from ethyl 2-cyano-3-(substituted phenyl) acrylates [24][25][26][27][28][29][30][31][32][33][34].…”
Section: Introductionmentioning
confidence: 99%