Results 231 to 240 of about 12,719 (269)

Chlorosulfonation of 2-pyridones [PDF]

open access: possibleChemistry 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.
T. I. Likhomanova   +2 more
openaire   +1 more source

Pyridone photoelectrocyclizations to pyridophenanthrenes

Tetrahedron, 2017
Abstract This article describes the synthesis of pyridophenanthrenes from the stereoselective electrocyclization and [1,5]-hydride shift sequences of biphenyl pyridones. The regioselectivity of the reaction of meta-substituted biphenyl substrates depended on the electronic environment of the substituents.
Jon D. Rainier, Xuchen Zhao
openaire   +2 more sources

ChemInform Abstract: TAUTOMERIZATION OF FORMAMIDE, 2‐PYRIDONE, AND 4‐PYRIDONE: AN AB INITIO STUDY [PDF]

open access: possibleChemischer Informationsdienst, 1982
The tautomerism of formamide, 2-pyridone, and 4-pyridone has been investigated by ab initio calculations using minimal, extended, and polarization basis sets. When the effects of geometry optimization, polarization functions, correlation energy (estimated by second-order Merller-Plesset perturbation theory), and zero-point vibration energy are combined,
H. Bernhard Schlegel   +2 more
openaire   +2 more sources

Ring lithiation of pyridones

Journal of the Chemical Society, Perkin Transactions 1, 1988
AbstractTreatment of (I) with BuLi results in lithiation of the methyl group and formation of the dimer (II); 6‐lithiation represents a minor pathway (15% (III) is obtained on quenching with D2O).
Premji Meghani, John A. Joule
openaire   +3 more sources

Photochemical Reactivity of Pyridones

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
openaire   +2 more sources

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 ...
Herbert Mayr, Martin Breugst
openaire   +3 more sources

Unusual pyridone salts

Journal of the Chemical Society B: Physical Organic, 1968
The reaction between N-alkyl-2-pyridones and tetracyanoethylene produces 2 : 1 salts of the pyridone with pentacyanopropene. Metathetical exchange of these salts with 4H-quinolizin-4-one leads to mono- and bis-quinolizone salts. Similar salts are formed with hydroquinone in place of pentacyanopropene.
K. Rajagopalan   +2 more
openaire   +2 more sources

Pyridones as Potential Antitumor Agents

Journal of Pharmaceutical Sciences, 1979
AbstractDurch Persulfat‐Oxidation wird das Hydroxypyridin (I) in das Pyridon (II) übergeführt, aus dem das Acetylderivat (III) hergestellt wird.
John S. Driscoll, Deng Ruey Hwang
openaire   +4 more sources

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.
R. Ramaekers   +5 more
openaire   +2 more sources

Photoionization of 2-pyridone and 2-hydroxypyridine

Physical Chemistry Chemical Physics, 2010
We studied the photoionization of 2-pyridone and its tautomer, 2-hydroxypyridine by means of VUV synchrotron radiation coupled to a velocity map imaging electron/ion coincidence spectrometer. The photoionization efficiency (PIE) spectrum is composed of steps.
C. Poully, J.   +10 more
openaire   +4 more sources

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