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Bioconjugate Chemistry(1)
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Bioconjugation through Mesitylene Thiol Alkylation
ArticleAbstract: The design and generation of complex multifunctional macromolecular structures by bioconjugation isPalabras claves:Autores:Alberício F., Cuevas C., Domínguez J.M., Hortensia Rodriguez Cabrera, Pérez-Chacon G., Ramos-Tomillero I., Sánchez‐Madrid F., Somovilla-Crespo B., Zapata J.M.Fuentes:googlescopusA convenientmicrowave-enhanced solid-phase synthesis of short chain N-methyl-rich peptides
ArticleAbstract: Structural modification of the peptide backbone via N-methylation is a powerful tool to modulate thePalabras claves:Fmoc-N-methyl amino acids, MICROWAVE, Solid-phase peptide synthesisAutores:Alberício F., Hortensia Rodriguez Cabrera, Suárez Navarro M.Fuentes:scopusA study of the electrospray ionisation and ion-trap fragmentation of [M - H]<sup>-</sup> ions of new 3,5-disubstituted tetrahydro-2H-1,3,5-thiadiazin-2-thiones
ArticleAbstract: The electrospray ionisation (ESI) in negative mode of the pharmacologically significant 3,5-disubstiPalabras claves:Autores:Hortensia Rodriguez Cabrera, Kayali N., Martín N., Martínez-Álvarez R., Perez-Pineiro R., Seoane C., Suárez Navarro M.Fuentes:scopusUnderstanding Tetrahydropyranyl as a Protecting Group in Peptide Chemistry
ReviewAbstract: Tetrahydropyranyl (Thp) is recognized as a useful protecting group for alcohols in organic synthesisPalabras claves:3,4-dihydro-2H-pyran, hydroxyl groups, Protecting groups, tetrahydropyranyl group, ThiolsAutores:Alberício F., B. G. De la Torre, El-Faham A., Hortensia Rodriguez Cabrera, Nicolas E., Ramos-Tomillero I., Sharma A.Fuentes:googlescopusSolid-phase synthesis and structural study of substituted 1,4,5,6-tetrahydro-6-oxopyridine-3-carboxylic acids
ArticleAbstract: An efficient solid-phase approach to prepare substituted 1,4,5,6-tetrahydro-6-oxopyridines bearing aPalabras claves:1,4,5,6-Tetrahydro-6-oxopyridine-3-carboxylic acids, B3LYP/6-31G* theoretical calculations, solid-phase synthesis, Wang resinAutores:Alberício F., Garay H.E., Hortensia Rodriguez Cabrera, Martín N., Martín O., Ochoa E., Reyes O., Suárez Navarro M.Fuentes:scopusSolvent-free synthesis of 4-aryl substituted 5-alkoxycarbonyl-6-methyl-3,4-dihydropyridones under microwave irradiation
ArticleAbstract: 4-Aryl substituted 5-alkoxycarbonyl-6-methyl-3,4-dihydropyridones have been prepared in one-pot condPalabras claves:dihydropyridones, Microwave irradiation, Solvent-free synthesisAutores:Hortensia Rodriguez Cabrera, Loupy A., Perez-Pineiro R., Petit A., Suárez Navarro M.Fuentes:googlescopusSpectral Assignments and Reference Data<sup>1</sup>H and<sup>13</sup>C NMR spectral assignments for 3,5-disubstituted tetrahydro-2H-1,3,5-thiadiazine-2-thione derivatives
ArticleAbstract: The proton and carbon spectra of 3,5-disubstituted tetrahydro-2H-1,3,5-thiadiazine-2-thione derivatiPalabras claves:1 H NMR, 1,3,5-thiadiazine-2-thione, 13 C NMR, NMRAutores:Hortensia Rodriguez Cabrera, Martín N., Martinez R., Molero D., Perez-Pineiro R., Seoane C., Suárez Navarro M.Fuentes:scopusStructure-Acid Lability Relationship of N-alkylated α,α-dialkylglycine Obtained via a Ugi Multicomponent Reaction
ArticleAbstract: Using the classical Ugi four-component reaction to fuse an amine, ketone, carboxylic acid, and isocyPalabras claves:acidolysis study, N-alkylated α,α-dialkylglycine, structure-acid lability, Ugi multicomponent reactionAutores:Alberício F., Hortensia Rodriguez Cabrera, Marisa K. Sánchez, Ramos-Tomillero I.Fuentes:scopus