Cargando…
Cysteine Pseudoprolines for Thiol Protection and Peptide Macrocyclization Enhancement in Fmoc-Based Solid-Phase Peptide Synthesis
[Image: see text] Contrary to other studies, here we describe cysteine (Cys) pseudoproline-containing peptides with short deprotection times in TFA. The deprotection times fell in the same range as other protecting groups commonly used in SPPS (e.g., 1–3 h). Moreover, when using Cys pseudoprolines a...
Autores principales: | Postma, Tobias M., Albericio, Fernando |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2014
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971734/ https://www.ncbi.nlm.nih.gov/pubmed/24617568 http://dx.doi.org/10.1021/ol5004725 |
Ejemplares similares
-
Solid-Phase Synthesis
of an “Inaccessible”
hGH-Derived Peptide Using a Pseudoproline Monomer and SIT-Protection
for Cysteine
por: Manne, Srinivasa Rao, et al.
Publicado: (2022) -
Tea Bags for Fmoc Solid-Phase Peptide Synthesis: An Example of Circular Economy
por: Guzmán, Fanny, et al.
Publicado: (2021) -
Deprotection Reagents in Fmoc Solid Phase Peptide Synthesis: Moving Away from Piperidine?
por: Luna, Omar F., et al.
Publicado: (2016) -
Advances in Fmoc solid‐phase peptide synthesis
por: Behrendt, Raymond, et al.
Publicado: (2016) -
Optimized Stepwise Synthesis of the API Liraglutide
Using BAL Resin and Pseudoprolines
por: Carbajo, Daniel, et al.
Publicado: (2019)