Advances in the synthesis of 4-aryl- and 4-hetarylpyridines
Identifieur interne : 001051 ( Main/Exploration ); précédent : 001050; suivant : 001052Advances in the synthesis of 4-aryl- and 4-hetarylpyridines
Auteurs :Source :
- Russian Chemical Reviews [ 0036-021X ] ; 2008-12-31.
English descriptors
- KwdEn :
- Abstr, Acetic, Acetic acid, Acoh, Aldehyde, Ammonia, Ammonium, Ammonium acetate, Aqueous solution, Aromatic, Aromatic aldehydes, Aryl, Arylation, Benzene, Benzene ring, Bipyridyl, Bromide, Catalyst, Certain cases, Chalcone, Chem, Co2et, Corresponding pyridines, Derivative, Dioxane, Eto2c, Etoh, First stage, Fomina, Good yields, Grignard reagents, Gromov, Halide, Heterocyclic, High yields, Hydroxide, Inorg, Ketone, Kharash reaction, Krohnke, Krohnke method, Krohnke salt, Large series, Lett, Lithium, Methyl ketone, Methylammonium sulfite, Michael reaction, Mild conditions, Negishi reaction, Nh4oac, Nitrogen atom, Palladium, Palladium catalyst, Perkin trans, Phme, Precursor, Product yields, Pyridine, Pyridine derivatives, Pyridine ring, Pyridinium, Pyridinium salt, Reaction mechanism, Reaction products, Reagent, Room temperature, Sodium carbonate, Sodium hydroxide, Stille reaction, Substituents, Sulfite, Suzuki, Suzuki reaction, Synthesis, Terpyridines, Tetrahedron, Trifluoroacetic acid.
- Teeft :
- Abstr, Acetic, Acetic acid, Acoh, Aldehyde, Ammonia, Ammonium, Ammonium acetate, Aqueous solution, Aromatic, Aromatic aldehydes, Aryl, Arylation, Benzene, Benzene ring, Bipyridyl, Bromide, Catalyst, Certain cases, Chalcone, Chem, Co2et, Corresponding pyridines, Derivative, Dioxane, Eto2c, Etoh, First stage, Fomina, Good yields, Grignard reagents, Gromov, Halide, Heterocyclic, High yields, Hydroxide, Inorg, Ketone, Kharash reaction, Krohnke, Krohnke method, Krohnke salt, Large series, Lett, Lithium, Methyl ketone, Methylammonium sulfite, Michael reaction, Mild conditions, Negishi reaction, Nh4oac, Nitrogen atom, Palladium, Palladium catalyst, Perkin trans, Phme, Precursor, Product yields, Pyridine, Pyridine derivatives, Pyridine ring, Pyridinium, Pyridinium salt, Reaction mechanism, Reaction products, Reagent, Room temperature, Sodium carbonate, Sodium hydroxide, Stille reaction, Substituents, Sulfite, Suzuki, Suzuki reaction, Synthesis, Terpyridines, Tetrahedron, Trifluoroacetic acid.
Url:
DOI: 10.1070/RC2008v077n12ABEH003783
Affiliations:
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Le document en format XML
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<term>Aldehyde</term>
<term>Ammonia</term>
<term>Ammonium</term>
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<term>Catalyst</term>
<term>Certain cases</term>
<term>Chalcone</term>
<term>Chem</term>
<term>Co2et</term>
<term>Corresponding pyridines</term>
<term>Derivative</term>
<term>Dioxane</term>
<term>Eto2c</term>
<term>Etoh</term>
<term>First stage</term>
<term>Fomina</term>
<term>Good yields</term>
<term>Grignard reagents</term>
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<term>Halide</term>
<term>Heterocyclic</term>
<term>High yields</term>
<term>Hydroxide</term>
<term>Inorg</term>
<term>Ketone</term>
<term>Kharash reaction</term>
<term>Krohnke</term>
<term>Krohnke method</term>
<term>Krohnke salt</term>
<term>Large series</term>
<term>Lett</term>
<term>Lithium</term>
<term>Methyl ketone</term>
<term>Methylammonium sulfite</term>
<term>Michael reaction</term>
<term>Mild conditions</term>
<term>Negishi reaction</term>
<term>Nh4oac</term>
<term>Nitrogen atom</term>
<term>Palladium</term>
<term>Palladium catalyst</term>
<term>Perkin trans</term>
<term>Phme</term>
<term>Precursor</term>
<term>Product yields</term>
<term>Pyridine</term>
<term>Pyridine derivatives</term>
<term>Pyridine ring</term>
<term>Pyridinium</term>
<term>Pyridinium salt</term>
<term>Reaction mechanism</term>
<term>Reaction products</term>
<term>Reagent</term>
<term>Room temperature</term>
<term>Sodium carbonate</term>
<term>Sodium hydroxide</term>
<term>Stille reaction</term>
<term>Substituents</term>
<term>Sulfite</term>
<term>Suzuki</term>
<term>Suzuki reaction</term>
<term>Synthesis</term>
<term>Terpyridines</term>
<term>Tetrahedron</term>
<term>Trifluoroacetic acid</term>
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<term>Acetic</term>
<term>Acetic acid</term>
<term>Acoh</term>
<term>Aldehyde</term>
<term>Ammonia</term>
<term>Ammonium</term>
<term>Ammonium acetate</term>
<term>Aqueous solution</term>
<term>Aromatic</term>
<term>Aromatic aldehydes</term>
<term>Aryl</term>
<term>Arylation</term>
<term>Benzene</term>
<term>Benzene ring</term>
<term>Bipyridyl</term>
<term>Bromide</term>
<term>Catalyst</term>
<term>Certain cases</term>
<term>Chalcone</term>
<term>Chem</term>
<term>Co2et</term>
<term>Corresponding pyridines</term>
<term>Derivative</term>
<term>Dioxane</term>
<term>Eto2c</term>
<term>Etoh</term>
<term>First stage</term>
<term>Fomina</term>
<term>Good yields</term>
<term>Grignard reagents</term>
<term>Gromov</term>
<term>Halide</term>
<term>Heterocyclic</term>
<term>High yields</term>
<term>Hydroxide</term>
<term>Inorg</term>
<term>Ketone</term>
<term>Kharash reaction</term>
<term>Krohnke</term>
<term>Krohnke method</term>
<term>Krohnke salt</term>
<term>Large series</term>
<term>Lett</term>
<term>Lithium</term>
<term>Methyl ketone</term>
<term>Methylammonium sulfite</term>
<term>Michael reaction</term>
<term>Mild conditions</term>
<term>Negishi reaction</term>
<term>Nh4oac</term>
<term>Nitrogen atom</term>
<term>Palladium</term>
<term>Palladium catalyst</term>
<term>Perkin trans</term>
<term>Phme</term>
<term>Precursor</term>
<term>Product yields</term>
<term>Pyridine</term>
<term>Pyridine derivatives</term>
<term>Pyridine ring</term>
<term>Pyridinium</term>
<term>Pyridinium salt</term>
<term>Reaction mechanism</term>
<term>Reaction products</term>
<term>Reagent</term>
<term>Room temperature</term>
<term>Sodium carbonate</term>
<term>Sodium hydroxide</term>
<term>Stille reaction</term>
<term>Substituents</term>
<term>Sulfite</term>
<term>Suzuki</term>
<term>Suzuki reaction</term>
<term>Synthesis</term>
<term>Terpyridines</term>
<term>Tetrahedron</term>
<term>Trifluoroacetic acid</term>
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