Tsouker P.
18
Coauthors
3
Documentos
Volumen de publicaciones por año
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| Año de publicación | Num. Publicaciones |
|---|---|
| 2004 | 1 |
| 2006 | 2 |
Publicaciones por áreas de conocimiento
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| Área de conocimiento | Num. Publicaciones |
|---|---|
| Química orgánica | 3 |
| Bioquímica | 1 |
| Química general | 1 |
| Ingeniería química | 1 |
Publicaciones por áreas temáticas
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| Área temática | Num. Publicaciones |
|---|---|
| Química orgánica | 3 |
| Química inorgánica | 1 |
| Farmacología y terapéutica | 1 |
Principales fuentes de datos
| Origen | Num. Publicaciones |
|---|---|
| Scopus | 3 |
| Google Scholar | 3 |
| RRAAE | 0 |
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Coautores destacados por número de publicaciones
| Coautor | Num. Publicaciones |
|---|---|
| Koksch B. | 3 |
| Jan Spengler | 3 |
| Hennig L. | 3 |
| Burger K. | 3 |
| Alberício F. | 2 |
| El-Kousy S.M. | 1 |
| Lange T. | 1 |
| Osipov S.N. | 1 |
| Berger S. | 1 |
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Publicaciones del autor
Domino reactions with fluorinated five-membered heterocycles. α-Trifluoromethyl α-amino acids with unsaturated side-chains
ArticleAbstract: α-Trifluoromethyl α-amino acids with unsaturated side-chains have been prepared from 5-fluoro-4-trifPalabras claves:5-Fluoro-4-trifluoromethyloxazoles, Allyl alcohols, Claisen rearrangement, Farnesol, Geraniol, nucleophilic aromatic substitution, Propargyl alcohols, secondary structure, α-Trifluoromethyl α-amino acidsAutores:Alberício F., Burger K., Hennig L., Jan Spengler, Koksch B., Tsouker P.Fuentes:googlescopusSynthesis of α-trifluoromethyl α-amino acids with aromatic, heteroaromatic and ferrocenyl subunits in the side chain
ArticleAbstract: 5-Benzyloxy-4-trifluoromethyl-1,3-oxazoles, obtained from 5-fluoro-4-trifluoromethyloxazoles and benPalabras claves:1,3-Benzyl group migration versus Claisen rearrangement, 5-Fluoro-4-trifluoromethyl-1,3-oxazoles, Nucleophilic heteroaromatic substitution, Synthetic Tfm-Gly equivalent, α-Trifluoromethylamino acidsAutores:Alberício F., Burger K., Hennig L., Jan Spengler, Koksch B., Tsouker P.Fuentes:googlescopusHexafluoroacetone as a protecting and activating reagent: Synthesis of new types of fluoro-substituted α-amino, α-hydroxy and α-mercapto acids
ArticleAbstract: Starting from (S)-aspartic, (S)-malic, (S)-citramalic and (S,R)-thiomalic acid, new types of 4,4-difPalabras claves:amino acids, Fluorine, Hydroxy acids, Mercapto acids, PeptidesAutores:Berger S., Burger K., El-Kousy S.M., Hennig L., Jan Spengler, Koksch B., Lange T., Osipov S.N., Tsouker P.Fuentes:googlescopus