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ChemInform Abstract: PHOTOISOMERIZATION OF 4‐PYRIDONES TO 2‐PYRIDONES

Chemischer Informationsdienst, 1974
AbstractBestrahlung (Hg‐Mitteldrucklampe) der 4‐Pyridone (I) liefert die isomeren 2‐Pyridone (II) als Hauptprodukte, während die 4‐Pyridone (III) unter gleichen Bedingungen unverändert bleiben.
NOBUYUKI ISHIBE, JUN MASUI
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Lithiation of pyridones

Journal of the Chemical Society, Chemical Communications, 1985
Lithiation of 1-methyl-4-pyridone with n-butyl-lithium at -78 °C proceeds smoothly at the C-2 position and 2-substituted-4-pyridones (1c–j) are obtained by subsequent reaction with electorphiles; lithiation of 1-methyl-2-pyridone takes place predominantly at the N-methyl, the lithio-derivative reacting rapidly, even at -78 °C with starting pyridone to ...
Premji Patel, John A. Joule
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Pyridones as Potential Antitumor Agents

Journal of Pharmaceutical Sciences, 1979
Based on the finding that 3-acetoxy-2-pyridone had reproducible activity against murine P-388 lymphocytic leukemia, derivatives in this series were synthesized and evaluated to determine structural parameters important for activity. Of the 32 compounds tested, 10 were active.
D R, Hwang, J S, Driscoll
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Ambident Reactivities of Pyridone Anions

Journal of the American Chemical Society, 2010
The kinetics of the reactions of the ambident 2- and 4-pyridone anions with benzhydrylium ions (diarylcarbenium ions) and structurally related Michael acceptors have been studied in DMSO, CH(3)CN, and water. No significant changes of the rate constants were found when the counterion was varied (Li(+), K(+), NBu(4)(+)) or the solvent was changed from ...
Martin, Breugst, Herbert, Mayr
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Tetrachlorobis(2-pyridone)-bis(μ2-2-pyridone)-dicopper

Acta Crystallographica Section C Crystal Structure Communications, 1993
In this structure two Cu II centres 3.4448 (11) A apart are bridged asymmetrically by two 2-pyridone ligands and each is further coordinated by three terminal ligands (two chlorides and one 2-pyridone). Each molecule has an approximate, non-crystallographic centre of symmetry.
A. J. Blake, R. E. P. Winpenny
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DFT/B3-LYP study of the hydrogen-bonding cooperativity: application to (2-pyridone)2, 2-pyridone–H2O, 2-pyridone–CH3OH and 2-pyridone–CH3OCH3

Chemical Physics Letters, 2000
Abstract DFT/B3-LYP(6-31++G**) calculations are used to provide information on closed N – H ⋯ O H -bonded complexes, containing two hydrogen bonds. The studied model systems with two H-bonds are the 2-pyridone dimer, 2-pyridone–H2O and 2-pyridone–CH3OH.
A. Dkhissi   +4 more
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Chlorosulfonation of 2-pyridones

Chemistry of Heterocyclic Compounds, 1974
Chlorosulfonlyl-substituted 2-pyridones were obtained for the first time. The ability of 2-pyridone-3-sulfonyl chlorides to undergo conversion to sulfonylides of the pyridine series by the action of bases is shown in the case of 5,6,7,8-tetrahydro-2-quinolone-3-sulfonyl chloride.
N. P. Shusherina   +2 more
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Pyridone‐Doped Acenes with Improved Stability

Chemistry – A European Journal, 2023
AbstractBesides the peripheral modification, the introduction of heteroatoms to modulate the property of longer acenes with improved chemical stability has been extensively studied for their potential applications in organic electronics. However, the utilization of 4‐pyridone, a common unit in the air‐ and photo‐stable acridone and quinacridone, to ...
Chengguo Yan, Weiwei Ding, Gang Zhang
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Electroorganic Oxidation of Pyridones

ECS Meeting Abstracts, 2018
Electroorganic synthesis can be utilized as a green alternative in complex organic synthesis reactions for pharmaceutical compounds, mitigating or eliminating complex stoichiometric oxidants during organic synthesis. An electrochemical oxidation reaction can make a synthetic transformation more cost effective and more efficient when compared to ...
Dylan Daniel Rodene   +4 more
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Photochemical Reactivity of Pyridones

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
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