
Fernandez-Llamazares A.I.
25
Coauthors
7
Documentos
Volumen de publicaciones por año
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Año de publicación | Num. Publicaciones |
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2010 | 1 |
2013 | 3 |
2014 | 2 |
2015 | 1 |
Publicaciones por áreas de conocimiento
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Área de conocimiento | Num. Publicaciones |
---|---|
Bioquímica | 7 |
Péptido | 5 |
Farmacología | 1 |
Ingeniería química | 1 |
Química analítica | 1 |
Publicaciones por áreas temáticas
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Área temática | Num. Publicaciones |
---|---|
Química orgánica | 4 |
Farmacología y terapéutica | 4 |
Química física | 2 |
Bioquímica | 2 |
Ingeniería química | 1 |
Química analítica | 1 |
Principales fuentes de datos
Origen | Num. Publicaciones |
---|---|
Scopus | 7 |
Google Scholar | 7 |
RRAAE | 0 |
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Coautores destacados por número de publicaciones
Coautor | Num. Publicaciones |
---|---|
Alberício F. | 7 |
Jan Spengler | 7 |
García J. | 2 |
Adan J. | 2 |
Mitjans F. | 2 |
Pérez-Tomás R. | 1 |
Soto-Cerrato V. | 1 |
Meunier D. | 1 |
Ruíz-Rodríguez J. | 1 |
Burger K. | 1 |
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Top Keywords
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Publicaciones del autor
Use of an internal reference for the quantitative HPLC-UV analysis of solid-phase reactions: A case study of 2-chlorotrityl chloride resin
ArticleAbstract: Here we evaluated the use of internal reference compounds for the rapid assessment of reactions perfPalabras claves:analytical construct, Barlos-Resin, DKP-formation, internal standard, reporter compoundAutores:Alberício F., Fernandez-Llamazares A.I., Jan SpenglerFuentes:googlescopusReview Backbone N-Modified Peptides: How to Meet the Challenge of Secondary Amine Acylation
ArticleAbstract: Backbone N-substitution of peptides (N-Me and N-alkyl) has become of special interest as a chemicalPalabras claves:acylation, coupling reagent, methylationAutores:Alberício F., Fernandez-Llamazares A.I., Jan SpenglerFuentes:googlescopusThe potential of N-alkoxymethyl groups as peptide backbone protectants
ArticleAbstract: In this study, the potential of N-alkoxymethyl groups as protectants for the peptide backbone has bePalabras claves:Backbone N-alkylation, Backbone protecting groups, N-Alkoxymethyl, Peptides, SPPSAutores:Alberício F., Fernandez-Llamazares A.I., Jan SpenglerFuentes:googlescopusTackling lipophilicity of peptide drugs: Replacement of the backbone n -methyl group of Cilengitide by N -oligoethylene glycol (N -OEG) chains
ArticleAbstract: Cilengitide is an RGD-peptide of sequence cyclo[RGDfNMeV] that was was developed as a highly activePalabras claves:Autores:Adan J., Alberício F., Fernandez-Llamazares A.I., Jan Spengler, Mitjans F.Fuentes:googlescopusTotal regioselective control of tartaric acid
ArticleAbstract: An efficient strategy to synthesize tartaric acid building blocks for totally regioselective transfoPalabras claves:Autores:Alberício F., Burger K., Fernandez-Llamazares A.I., Jan Spengler, Ruíz-Rodríguez J.Fuentes:googlescopus