Böttcher C.
17
Coauthors
5
Documentos
Volumen de publicaciones por año
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Año de publicación | Num. Publicaciones |
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2004 | 2 |
2005 | 2 |
2006 | 1 |
Publicaciones por áreas de conocimiento
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Área de conocimiento | Num. Publicaciones |
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Bioquímica | 6 |
Química orgánica | 1 |
Ingeniería química | 1 |
Carbohidratos | 1 |
Descubrimiento de fármacos | 1 |
Farmacología | 1 |
Péptido | 1 |
Ciencia de materiales | 1 |
Publicaciones por áreas temáticas
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Área temática | Num. Publicaciones |
---|---|
Química analítica | 3 |
Química orgánica | 2 |
Técnicas, equipos y materiales | 1 |
Farmacología y terapéutica | 1 |
Principales fuentes de datos
Origen | Num. Publicaciones |
---|---|
Scopus | 5 |
Google Scholar | 5 |
RRAAE | 0 |
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Coautores destacados por número de publicaciones
Coautor | Num. Publicaciones |
---|---|
Jan Spengler | 5 |
Burger K. | 5 |
Alberício F. | 3 |
Hennig L. | 2 |
Essawy S.A. | 1 |
Radics G. | 1 |
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Publicaciones del autor
Hexafluoroacetone as protecting and activating reagent. Glycosylated malic, citramalic, and thiomalic acid derivatives, new glycosylated building blocks for drug design
ArticleAbstract: Glycosylated α-hydroxy and α-mercapto acids have been synthesized starting from malic/citramalic/thiPalabras claves:3-Hydroxysuccinimido sugars, Dielectrophiles, Glycosylamines, Maleimido sugars, N-Glycosylated depsipeptides, α-Hydroxy acids, α-Hydroxyacylamino acids, α-Mercapto acids, α-Mercaptoacylamino acidsAutores:Böttcher C., Burger K., Jan SpenglerFuentes:googlescopusHexafluoroacetone as protecting and activating reagent. A new approach to N-glycosides
ArticleAbstract: N-Glycosides of Asn and homologues have been synthesized starting from hexafluoroacetone-protected ωPalabras claves:Dielectrophiles, Hexafluoroacetone, N-Glycopeptides, N-Glycosylamino acids, N-glycosylationAutores:Böttcher C., Burger K., Essawy S.A., Jan SpenglerFuentes:googlescopusHexafluoroacetone as protecting and activating reagent: New routes to amino, hydroxy, and mercapto acids and their application for peptide and glyco- and depsipeptide modification
ArticleAbstract: A critical overview is given of the synthetic potential of hexafluoroacetone (HFA) as bidentate reagPalabras claves:Autores:Alberício F., Böttcher C., Burger K., Jan SpenglerFuentes:googlescopusHexafluoroacetone as a protecting and activating reagent. N- and O-glycosylation of isoserine and isocysteine *
ArticleAbstract: Starting from HFA-protected malic and thiomalic acid a series of O- and N-glycoconjugates suitable fPalabras claves:Glycoconjugates, Glycosylamines, Hexafluoroacetone, Isocyanates, malic acid, Thiomalic acidAutores:Alberício F., Böttcher C., Burger K., Hennig L., Jan SpenglerFuentes:googlescopusOrthogonally protected, carboxy-activated L-homoisoserine, 2-methyl-L-homoisoserine, and homoisocysteine derivatives. New building blocks for peptide and depsipeptide modification
ArticleAbstract: Starting from L-malic, L-citramalic, and rac. thiomalic acids routes to L-homoisoserine, 2-methyl-L-Palabras claves:Arndt-Eistert reaction, Azapeptides, Citramalic acid, Curtius rearrangement, Depsipeptide modification, Hexafluoroacetone, malic acid, Peptide modification, Thiomalic acid, Wolff rearrangement, α-Hydroxy acids, α-Mercapto acids, γ-Amino acidsAutores:Alberício F., Böttcher C., Burger K., Hennig L., Jan Spengler, Radics G.Fuentes:googlescopus