Cargando…
Macrocyclisation of small peptides enabled by oxetane incorporation
Cyclic peptides are an important source of new drugs but are challenging to produce synthetically. We show that head-to-tail peptide macrocyclisations are greatly improved, as measured by isolated yields, reaction rates and product distribution, by substitution of one of the backbone amide C[double...
Autores principales: | Roesner, Stefan, Saunders, George J., Wilkening, Ina, Jayawant, Eleanor, Geden, Joanna V., Kerby, Paul, Dixon, Ann M., Notman, Rebecca, Shipman, Michael |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385813/ https://www.ncbi.nlm.nih.gov/pubmed/30881675 http://dx.doi.org/10.1039/c8sc05474f |
Ejemplares similares
-
Photochemical Methods for Peptide Macrocyclisation
por: Raynal, Laetitia, et al.
Publicado: (2020) -
Asymmetric Synthesis of 2-Substituted
Oxetan-3-ones
via Metalated SAMP/RAMP Hydrazones
por: Geden, Joanna V., et al.
Publicado: (2013) -
Divergent unprotected peptide macrocyclisation by palladium-mediated cysteine arylation
por: Rojas, Anthony J., et al.
Publicado: (2017) -
Self-cyclisation as a general and efficient platform for peptide and protein macrocyclisation
por: Jia, Xinying, et al.
Publicado: (2023) -
Chemical Space Exploration of Oxetanes
por: Alves, Fernando Rodrigues de Sá, et al.
Publicado: (2020)