Results 231 to 240 of about 20,827 (302)
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Organic Letters, 2021
Co(III)-catalyzed highly regio- and stereoselective direct C6 olefination of 2-pyridones with alkynes has been developed with the assistance of chelation.
Xin Xu +8 more
semanticscholar +1 more source
Co(III)-catalyzed highly regio- and stereoselective direct C6 olefination of 2-pyridones with alkynes has been developed with the assistance of chelation.
Xin Xu +8 more
semanticscholar +1 more source
Chemo- and Enantioselective Insertion of Furyl Carbene into the N-H Bond of 2-Pyridones.
Angewandte Chemie, 2021Asymmetric carbene insertion reactions represent one of the most important protocols to construct carbon-heteroatom bonds. The use of donor-acceptor diazo compounds bearing an ester group is however a prerequisite for achieving high enantioselectivity ...
Kai Wang +7 more
semanticscholar +1 more source
Organic Letters, 2021
An operationally simple protocol for direct N- and O-difluoromethylation of 2-pyridones, quinolinones, and isoquinolinones using commercially available TMSCF2Br is disclosed. The chemoselectivity is modulated by simple variations in temperature, solvent,
Ziyue Zhu +4 more
semanticscholar +1 more source
An operationally simple protocol for direct N- and O-difluoromethylation of 2-pyridones, quinolinones, and isoquinolinones using commercially available TMSCF2Br is disclosed. The chemoselectivity is modulated by simple variations in temperature, solvent,
Ziyue Zhu +4 more
semanticscholar +1 more source
Journal of Organic Chemistry, 2021
The highly regioselective N-alkylation reaction of 2-pyridones was achieved through hydrazone chemistry, especially for substrates with bulky secondary alkyl groups.
Ye-bin Wu +6 more
semanticscholar +1 more source
The highly regioselective N-alkylation reaction of 2-pyridones was achieved through hydrazone chemistry, especially for substrates with bulky secondary alkyl groups.
Ye-bin Wu +6 more
semanticscholar +1 more source
Organic Letters, 2021
A new asymmetric catalytic protocol for the synthesis of enantioenriched N-allyl 2-pyrodones has been developed via the first Pd-catalyzed regio- and enantioselective aminoarylation of allenols with aryl iodides and 2-pyridones.
Hongfang Li +6 more
semanticscholar +1 more source
A new asymmetric catalytic protocol for the synthesis of enantioenriched N-allyl 2-pyrodones has been developed via the first Pd-catalyzed regio- and enantioselective aminoarylation of allenols with aryl iodides and 2-pyridones.
Hongfang Li +6 more
semanticscholar +1 more source
, 2021
Conventional C–H alkenylation with alkynes via low-valent transition-metal catalysis occurs at the C6 or C4 position of 2-pyridone with electron-deficient C–H bonds.
Ge Yin +6 more
semanticscholar +1 more source
Conventional C–H alkenylation with alkynes via low-valent transition-metal catalysis occurs at the C6 or C4 position of 2-pyridone with electron-deficient C–H bonds.
Ge Yin +6 more
semanticscholar +1 more source
4-Hydroxy Pyridones from Heterologous Expression and Cultivation of the Native Host.
Journal of Natural Products, 20204-Hydroxy pyridones are a class of fungi-derived polyketide-nonribosomal peptide products featuring a core of 4-hydroxy-2-pyridone which have a wide range of biological activities.
Wei-Yang Zhang +12 more
semanticscholar +1 more source
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.
A. J. Blake, R. E. P. Winpenny
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Pyridones as Potential Antitumor Agents II: 4-Pyridones and Bioisosteres of 3-Acetoxy-2-pyridone
Journal of Pharmaceutical Sciences, 1980Pyridone structural requirements for activity against murine P-388 leukemia have been extended to isosteric analogs of 3-hydroxy-4-pyridone, a compound previously found to have activity. An amino group can be substituted for the 3-hydroxyl function with retention of activity.
D R, Hwang, G R, Proctor, J S, Driscoll
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