Tertiary alkylamines as nucleophiles in substitution reactions at heteroaromatic halide during the synthesis of the highly potent pirinixic acid derivative 2-(4-chloro-6-(2,3-dimethylphenylamino)pyrimidin-2-ylthio)octanoic acid (YS-121)
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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In: Molecules, 16.2011, Heft 12, S. 10013-10028, doi:10.3390/molecules161210013
- Classification
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Chemie
- Event
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Veröffentlichung
- (where)
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Frankfurt am Main
- (who)
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Universitätsbibliothek Johann Christian Senckenberg
- (when)
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2011
- Creator
- URN
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urn:nbn:de:hebis:30:3-253130
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 14.08.2025, 10:47 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Gabler, Matthias
- Schubert-Zsilavecz, Manfred
- Universitätsbibliothek Johann Christian Senckenberg
Time of origin
- 2011
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Reactivity of oxygen and sulfur nucleophiles and basicity scales toward heteroatom Lewis acids
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Exploring the Catalytic Promiscuity of Phenolic Acid Decarboxylases: Asymmetric, 1,6‐Conjugate Addition of Nucleophiles Across 4‐Hydroxystyrene
Synthese von Pyrrolo[2,3-d]pyrimidin [Pyrrolo-d-pyrimidin] und Pyrazolo[3,4-d]pyrimidin-2'-Desoxyribofuranosiden [Pyrazolo-d-pyrimidin-Desoxyribofuranosiden] unter Phasentransferbedingungen
Stereoselective oxidative glycosylation of anomeric nucleophiles with alcohols and carboxylic acids
Metabolism of 2,4-dichlorophenoxyacetic acid, 4-chloro-2-methylphenoxyacetic acid and 2-methylphenoxyacetic acid by Alcaligenes eutrophus JMP 134
Reactivity of oxygen and sulfur nucleophiles and basicity scales toward heteroatom Lewis acids
Perhalogenated pyrimidine scaffolds. Reactions of 5-chloro-2,4,6-trifluoropyrimidine with nitrogen centred nucleophiles
Triflic Acid‐Catalyzed Dehydrative Amination of 2‐Arylethanols with Weak N ‐Nucleophiles in Hexafluoroisopropanol
Triflic Acid‐Catalyzed Dehydrative Amination of 2‐Arylethanols with Weak N ‐Nucleophiles in Hexafluoroisopropanol
Access to 2-oxoazetidine-3-carboxylic acid derivatives via thermal microwave-assisted Wolff rearrangement of 3-diazotetramic acids in the presence of nucleophiles
Neue Pyrimidin-Synthesen
Controlling Antibacterial Activity Exclusively with Visible Light: Introducing a Tetra‐ ortho ‐Chloro‐Azobenzene Amino Acid
The Hydrogen‐Bond Continuum in the Salt/Cocrystal Systems of Quinoline and Chloro‐Nitrobenzoic Acids
Exploring the Catalytic Promiscuity of Phenolic Acid Decarboxylases: Asymmetric, 1,6‐Conjugate Addition of Nucleophiles Across 4‐Hydroxystyrene
Synthese von Pyrrolo[2,3-d]pyrimidin [Pyrrolo-d-pyrimidin] und Pyrazolo[3,4-d]pyrimidin-2'-Desoxyribofuranosiden [Pyrazolo-d-pyrimidin-Desoxyribofuranosiden] unter Phasentransferbedingungen
Stereoselective oxidative glycosylation of anomeric nucleophiles with alcohols and carboxylic acids
Metabolism of 2,4-dichlorophenoxyacetic acid, 4-chloro-2-methylphenoxyacetic acid and 2-methylphenoxyacetic acid by Alcaligenes eutrophus JMP 134
Reactivity of oxygen and sulfur nucleophiles and basicity scales toward heteroatom Lewis acids
Perhalogenated pyrimidine scaffolds. Reactions of 5-chloro-2,4,6-trifluoropyrimidine with nitrogen centred nucleophiles
Triflic Acid‐Catalyzed Dehydrative Amination of 2‐Arylethanols with Weak N ‐Nucleophiles in Hexafluoroisopropanol
Triflic Acid‐Catalyzed Dehydrative Amination of 2‐Arylethanols with Weak N ‐Nucleophiles in Hexafluoroisopropanol
Access to 2-oxoazetidine-3-carboxylic acid derivatives via thermal microwave-assisted Wolff rearrangement of 3-diazotetramic acids in the presence of nucleophiles
Neue Pyrimidin-Synthesen
Controlling Antibacterial Activity Exclusively with Visible Light: Introducing a Tetra‐ ortho ‐Chloro‐Azobenzene Amino Acid
The Hydrogen‐Bond Continuum in the Salt/Cocrystal Systems of Quinoline and Chloro‐Nitrobenzoic Acids
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