Mostrando 7 resultados de: 7
Filtros aplicados
Subtipo de publicación
Article(7)
Publisher
European Journal of Organic Chemistry(2)
Organic and Biomolecular Chemistry(2)
Amino Acids(1)
ChemMedChem(1)
Molecules(1)
Área temáticas
Química orgánica(3)
Farmacología y terapéutica(2)
Enfermedades(1)
Funcionamiento de bibliotecas y archivos(1)
Organizaciones generales en Norteamérica(1)
1,3,5-Triazino Peptide Derivatives: Synthesis, Characterization, and Preliminary Antileishmanial Activity
ArticleAbstract: A library of short di-, tri-, and tetra-peptides with an s-triazine moiety at the N terminus and eitPalabras claves:1,3,5-triazine derivatives, antileishmanial compounds, morpholines, Peptides, piperidinesAutores:Abd El-Rahman M.M., Alberício F., B. G. De la Torre, Bekhit A.A., El-Faham A., Khalil H.H., Khattab S.N.Fuentes:scopus2-Methyltetrahydrofuran and cyclopentyl methyl ether for green solid-phase peptide synthesis
ArticleAbstract: 2-MeTHF and CPME were evaluated as greener alternatives for the most employed solvents in peptide syPalabras claves:2-methyltetrahydrofuran, Cyclopentyl methyl ether, Green solvents, Peptide synthesis, Solid-phase peptide synthesisAutores:Acosta G.A., Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Khattab S.N., Kruger H.G.Fuentes:scopusEDC·HCl and Potassium Salts of Oxyma and Oxyma-B as Superior Coupling Cocktails for Peptide Synthesis
ArticleAbstract: Nowadays, DIC is the most widely used carbodiimide for solid-phase peptide synthesis, while EDC·HClPalabras claves:peptide coupling, Peptides, solid-phase synthesis, Steric hindrance, synthetic methodsAutores:Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Khattab S.N., Kruger H.G.Fuentes:scopusOxyma-B, an excellent racemization suppressor for peptide synthesis
ArticleAbstract: Peptide-bond formation is a key process in the synthesis of peptide oligomers. Among the many coupliPalabras claves:Autores:Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Khattab S.N., Kruger H.G.Fuentes:scopusPeptide synthesis beyond DMF: THF and ACN as excellent and friendlier alternatives
ArticleAbstract: To date, DMF has been considered as the only solvent suitable for peptide synthesis. Here we demonstPalabras claves:Autores:Acosta G.A., Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Khattab S.N., Kruger H.G.Fuentes:scopusK-Oxyma: A strong acylation-promoting, 2-ctc resin-friendly coupling additive
ArticleAbstract: Here we present a new formulation of the recently introduced OxymaPure additive for peptide bond forPalabras claves:Acid-labile solid supports, acylation, Peptides, solid-phase synthesisAutores: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.Fuentes:scopusTOMBU and COMBU as novel uronium-type peptide coupling reagents derived from oxyma-b
ArticleAbstract: Here we describe two novel uronium salts, TOMBU and COMBU, derived from the recently described OxymaPalabras claves:amino acids, Coupling reagents, Oxyma-B, Peptide synthesis, Solid-phase peptide synthesisAutores:Alberício F., B. G. De la Torre, El-Faham A., Govender T., Jad Y.E., Khattab S.N., Kruger H.G.Fuentes:scopus