Results 191 to 200 of about 16,008 (266)
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Organic Letters, 2020
A Rh-catalyzed chelation-assisted C6-selective C-H activation/alkylation of 2-pyridones with readily available alkyl carboxylic acids or anhydrides is introduced. The reaction proceeds via substrate decarbonylation.
Haoqiang Zhao+8 more
semanticscholar +1 more source
A Rh-catalyzed chelation-assisted C6-selective C-H activation/alkylation of 2-pyridones with readily available alkyl carboxylic acids or anhydrides is introduced. The reaction proceeds via substrate decarbonylation.
Haoqiang Zhao+8 more
semanticscholar +1 more source
Tetrachlorobis(2-pyridone)-bis(μ2-2-pyridone)-dicopper
Acta Crystallographica Section C Crystal Structure Communications, 1993In 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.
R. E. P. Winpenny, A. J. Blake
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ChemInform Abstract: Synthesis of Pyridines and Pyridones.
Chemischer Informationsdienst, 1984AbstractDie Synthese einiger Furobenzopyranone, Pyridine und Pyridone auf Basis der Naturstoffe Visnagin und Khellin wird beschrieben.
Madiha M. Y. Zohair+2 more
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Journal of Organic Chemistry, 2020
We have identified different N-substituted 2-pyridones as inbuilt directing groups for selective C-H-activated functionalization instead of deprotecting and/or throwing away the directing groups.
Tanmay K Pati+5 more
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We have identified different N-substituted 2-pyridones as inbuilt directing groups for selective C-H-activated functionalization instead of deprotecting and/or throwing away the directing groups.
Tanmay K Pati+5 more
semanticscholar +1 more source
Journal of Organic Chemistry, 2020
A mild, catalyst- and metal-free photochemical protocol for the oxygenation of 3-cyano-1,4-dihydropyridines to 5-cyano-2-pyridones was developed. Utilizing molecular oxygen from air as the oxidant and a cheap blue LED lamp as the light source, a variety ...
Mengmeng Zhang+6 more
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A mild, catalyst- and metal-free photochemical protocol for the oxygenation of 3-cyano-1,4-dihydropyridines to 5-cyano-2-pyridones was developed. Utilizing molecular oxygen from air as the oxidant and a cheap blue LED lamp as the light source, a variety ...
Mengmeng Zhang+6 more
semanticscholar +1 more source
Pyridone photoelectrocyclizations to pyridophenanthrenes
Tetrahedron, 2017Abstract 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
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Chlorosulfonation of 2-pyridones [PDF]
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
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ChemInform Abstract: TAUTOMERIZATION OF FORMAMIDE, 2‐PYRIDONE, AND 4‐PYRIDONE: AN AB INITIO STUDY [PDF]
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
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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
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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
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Photochemical Reactivity of Pyridones
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
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