Cargando…
Copper-mediated peptide arylation selective for the N-terminus
Polypeptides present remarkable selectivity challenges for chemical methods. Amino groups are ubiquitous in polypeptide structure, yet few paradigms exist for reactivity and selectivity in arylation of amine groups. This communication describes the utilization of boronic acid reagents bearing certai...
Autores principales: | Miller, Mary K., Wang, Haopei, Hanaya, Kengo, Zhang, Olivia, Berlaga, Alex, Ball, Zachary T. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162437/ https://www.ncbi.nlm.nih.gov/pubmed/34094308 http://dx.doi.org/10.1039/d0sc02933e |
Ejemplares similares
-
A photochemical C=C cleavage process: toward access to backbone N-formyl peptides
por: Wang, Haopei, et al.
Publicado: (2021) -
A mechanistic investigation of the photoinduced, copper-mediated cross-coupling of an aryl thiol with an aryl halide
por: Johnson, Miles W., et al.
Publicado: (2016) -
Copper-catalyzed synthesis of 2-aminopyridylbenzoxazoles via domino reactions of intermolecular N-arylation and intramolecular O-arylation
por: Lu, Ju-You
Publicado: (2019) -
Ketoxime peptide ligations: oxidative couplings of alkoxyamines to N-aryl peptides
por: Guthrie, Quibria A. E., et al.
Publicado: (2019) -
Divergent unprotected peptide macrocyclisation by palladium-mediated cysteine arylation
por: Rojas, Anthony J., et al.
Publicado: (2017)