Mostrando 5 resultados de: 5
Filtros aplicados
Subtipo de publicación
Article(5)
Área temáticas
Química analítica(3)
Química orgánica(2)
Farmacología y terapéutica(1)
Técnicas, equipos y materiales(1)
Área de conocimiento
Bioquímica(5)
Carbohidratos(1)
Ciencia de materiales(1)
Descubrimiento de fármacos(1)
Farmacología(1)
Origen
scopus(5)
Hexafluoroacetone 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: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. 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: 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: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