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Chapter 15: Cyclic peptides as privileged structures
Book PartAbstract:Palabras claves:Autores:Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Jad Y.E., Kruger H.G., Ramesh S.Fuentes:scopusChemical platforms for peptide vaccine constructs
Book PartAbstract: Knowledge of the sequences and structures of proteins from pathogenic microorganisms has been put toPalabras claves:Chemical approaches, MAPS, Peptide epitopes, Synthesis, VaccineAutores:Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Kruger H.G., Ramesh S.Fuentes:scopusAn efficient solid-phase strategy for total synthesis of naturally occurring amphiphilic marine siderophores: Amphibactin-T and moanachelin ala-B
ArticleAbstract: Microorganisms such as bacteria, fungi and some plants secrete an abundance of suites of low moleculPalabras claves:Autores:Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Kruger H.G., Ramesh S.Fuentes:scopus6-(bromomaleimido)hexanoic acid as a connector for the construction of multiple branched peptide platforms
ArticleAbstract: We report on a novel and user-friendly platform based on a bromomaleimide moiety to obtain branchedPalabras claves:Autores:Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Kruger H.G., Ramesh S.Fuentes:scopusHighly chemoselective ligation of thiol- and amino-peptides on a bromomaleimide core
ArticleAbstract: Application of a bromomaleimide core allows for the incorporation of three different peptides. The kPalabras claves:Autores:Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Kruger H.G., Ramesh S.Fuentes:scopusImmobilized coupling reagents: Synthesis of amides/peptides
ReviewAbstract: The primary idea of using immobilized reagents in organic synthetic chemistry is to simplify the dowPalabras claves:combinatorial chemistry, coupling additive, high-throughput organic synthesis, solid-phase synthesis, stand-alone coupling reagentAutores:Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Kruger H.G., Ramesh S.Fuentes:scopusMicroreactors for peptide synthesis: Looking through the eyes of twenty first century!!!
OtherAbstract: The twenty first century has witnessed several advances in synthetic chemistry, among them microreacPalabras claves:Amide formation, Applications, Continuous flow, Microreactors, Peptide synthesisAutores:Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Kruger H.G., Ramesh S.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:scopusSolid-phase peptide synthesis (SPPS), C-terminal vs. side-chain anchoring: A reality or a myth
OtherAbstract: Here we review the strategies for the solid-phase synthesis of peptides starting from the side chainPalabras claves:C-terminal acid peptide, Side-chain anchoring, Solid-phase peptide synthesis, Stepwise elongationAutores:Acosta G.A., Alberício F., B. G. De la Torre, Cherkupally P., Govender T., Kruger H.G., Ramesh S.Fuentes:scopus