Cargando…
Chemoselective Late-Stage Functionalization of Peptides via Photocatalytic C2-Alkylation of Tryptophan
[Image: see text] Across eukaryotic proteomes, tryptophan is the least abundant of the 20 canonical amino acids, which makes it an ideal chemical handle for the late-stage functionalization of peptide and protein scaffolds with minimal production of undesired isoforms. Herein, we report the photocat...
Autores principales: | Lee, Joanna C., Cuthbertson, James D., Mitchell, Nicholas J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391624/ https://www.ncbi.nlm.nih.gov/pubmed/37462428 http://dx.doi.org/10.1021/acs.orglett.3c01795 |
Ejemplares similares
-
Reversible stapling of unprotected peptides via chemoselective methionine bis-alkylation/dealkylation
por: Shi, Xiaodong, et al.
Publicado: (2018) -
Modular synthesis of clickable peptides via late-stage maleimidation on C(7)-H tryptophan
por: Wang, Peng, et al.
Publicado: (2023) -
Late-stage peptide C–H alkylation for bioorthogonal C–H activation featuring solid phase peptide synthesis
por: Schischko, Alexandra, et al.
Publicado: (2019) -
Synthesis of 2-substituted tryptophans via a C3- to C2-alkyl migration
por: Mari, Michele, et al.
Publicado: (2014) -
Construction of diverse peptide structural architectures via chemoselective peptide ligation
por: Cheung, Carina Hey Pui, et al.
Publicado: (2021)