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Cleaving protected peptides from 2-chlorotrityl chloride resin. Moving away from dichloromethane
ArticleAbstract: In recent years, the work of various research groups has allowed the substitution of the hazardous sPalabras claves:Autores:Al Musaimi O., Alberício F., Alhassan M., B. G. De la Torre, Collins J.M.Fuentes:scopusGreening the Solid-Phase Peptide Synthesis Process. 2-MeTHF for the Incorporation of the First Amino Acid and Precipitation of Peptides after Global Deprotection
ArticleAbstract: In solid-phase peptide synthesis, dichloromethane is the predominant solvent used to incorporate thePalabras claves:2-MeTHF, Dipeptide formation, incorporation, precipitation, Racemization, Solid-phase peptide synthesisAutores:Al Musaimi O., Alberício F., B. G. De la Torre, Basso A., Collins J.M., El-Faham A., Jad Y.E., Kumar A.Fuentes:scopusInvestigating green ethers for the precipitation of peptides after global deprotection in solid-phase peptide synthesis
ReviewAbstract: Diethyl ether and methyl tert-butyl ether are the solvents most widely used for peptide precipitatioPalabras claves:Autores:Al Musaimi O., Alberício F., B. G. De la Torre, Basso A., Collins J.M., Jad Y.E., Kumar A.Fuentes:scopusPropylphosphonic Anhydride (T3P®) as Coupling Reagent for Solid-Phase Peptide Synthesis
ArticleAbstract: Amidation is the predominant reaction within the pharmaceutical setting, and it is attracting greatePalabras claves:Amidation, Green Chemistry, Peptides, SPPS, T3P ®Autores:Al Musaimi O., Alberício F., B. G. De la Torre, Talbiersky P., Wisdom R.Fuentes:scopus