Documentos de Alberício F. | REDI

Regresar

Mostrando 9 resultados de: 9

Filtros aplicados

Palabras Claves: "solid-phase synthesis"

Subtipo de publicación

Publisher

ACS Combinatorial Science(2)

ACS Sustainable Chemistry and Engineering(2)

European Journal of Organic Chemistry(2)

QSAR and Combinatorial Science(1)

Synthesis (Germany)(1)

Área temáticas

Química orgánica(4)

Farmacología y terapéutica(3)

Química analítica(3)

Química física(3)

Química inorgánica(2)

Área de conocimiento

Ingeniería química(4)

Ciencia de materiales(2)

Química orgánica(2)

Año de Publicación

Origen

Palabras Claves

Green Chemistry(2)

1,4,5,6-Tetrahydro-6-oxopyridine-3-carboxylic acids(1)

Acid-labile solid supports(1)

Calculating Resin Functionalization in Solid-Phase Peptide Synthesis Using a Standardized Method based on Fmoc Determination

Abstract: Solid-phase synthesis is the method of choice for peptide preparation in both research and industria

Palabras claves:

Fmoc, resin functionalization, solid-phase synthesis, standardization

Al Musaimi O., Alberício F., B. G. De la Torre, Basso A.

Green Solid-Phase Peptide Synthesis 2. 2-Methyltetrahydrofuran and Ethyl Acetate for Solid-Phase Peptide Synthesis under Green Conditions

Abstract: N,N-Dimethylformamide (DMF), N-methyl-2-pyrrolidone, and dichloromethane (DCM) are the most widely u

Palabras claves:

2-MeTHF, Green Chemistry, Peptide aggregation, Polyethylene glycol resins, Solid-phase peptide synthesis, solid-phase synthesis

Acosta G.A., Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Kruger H.G.

Green Transformation of Solid-Phase Peptide Synthesis

Abstract: Peptides play key roles in medicinal chemistry, being found in therapeutics and diagnostic agents, a

Palabras claves:

Green Chemistry, Green solvents, Parallel synthesis, Peptide synthesis, solid-phase synthesis

Alberício F., B. G. De la Torre, El-Faham A., Jad Y.E., Kumar A.

EDC·HCl and Potassium Salts of Oxyma and Oxyma-B as Superior Coupling Cocktails for Peptide Synthesis

Abstract: Nowadays, DIC is the most widely used carbodiimide for solid-phase peptide synthesis, while EDC·HCl

Palabras claves:

peptide coupling, Peptides, solid-phase synthesis, Steric hindrance, synthetic methods

Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Khattab S.N., Kruger H.G.

OxymaPure Coupling Reagents: Beyond Solid-Phase Peptide Synthesis

Abstract: OxymaPure [ethyl 2-cyano-2-(hydroxyimino)acetate] is an exceptional reagent with which to suppress r

Palabras claves:

amide bonds, coupling reagent, Peptides, Racemization, solid-phase synthesis

Alberício F., B. G. De la Torre, El-Faham A., Manne S.R.

Immobilized coupling reagents: Synthesis of amides/peptides

Abstract: The primary idea of using immobilized reagents in organic synthetic chemistry is to simplify the dow

Palabras claves:

combinatorial chemistry, coupling additive, high-throughput organic synthesis, solid-phase synthesis, stand-alone coupling reagent

Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Kruger H.G., Ramesh S.

K-Oxyma: A strong acylation-promoting, 2-ctc resin-friendly coupling additive

Abstract: Here we present a new formulation of the recently introduced OxymaPure additive for peptide bond for

Palabras claves:

Acid-labile solid supports, acylation, Peptides, solid-phase synthesis

Acosta G.A., Alberício F., Cherkupally P., El-Faham A., Hortensia Rodriguez Cabrera, Jan Spengler, Khattab S.N., Luxembourg Y., Nieto-Rodriguez L., Prohens R., Shamis M., Subiros-Funosas R.

Solid-phase N-glycopeptide synthesis using allyl side-chain protected Fmoc-amino acids

Abstract: A method for the preparation of glycopeptides using a three-dimensional orthogonal solid-phase strat

Palabras claves:

allyl esters, glycopeptides, Orthogonal protection, solid-phase synthesis

Alberício F., B. G. De la Torre, Eritja R., Kates S.

Solid-phase synthesis and structural study of substituted 1,4,5,6-tetrahydro-6-oxopyridine-3-carboxylic acids

Abstract: An efficient solid-phase approach to prepare substituted 1,4,5,6-tetrahydro-6-oxopyridines bearing a

Palabras claves:

1,4,5,6-Tetrahydro-6-oxopyridine-3-carboxylic acids, B3LYP/6-31G* theoretical calculations, solid-phase synthesis, Wang resin

Alberício F., Garay H.E., Hortensia Rodriguez Cabrera, Martín N., Martín O., Ochoa E., Reyes O., Suárez Navarro M.