Cargando…
Mechanistic investigation of aziridine aldehyde-driven peptide macrocyclization: the imidoanhydride pathway
Aziridine aldehyde dimers, peptides, and isocyanides participate in a multicomponent reaction to yield peptide macrocycles. We have investigated the selectivity and kinetics of this process and performed a detailed analysis of its chemoselectivity. While the reactants encompass all of the elements o...
Autores principales: | Zaretsky, Serge, Hickey, Jennifer L., Tan, Joanne, Pichugin, Dmitry, St. Denis, Megan A., Ler, Spencer, Chung, Benjamin K. W., Scully, Conor C. G., Yudin, Andrei K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949604/ https://www.ncbi.nlm.nih.gov/pubmed/29861887 http://dx.doi.org/10.1039/c5sc01958c |
Ejemplares similares
-
The reactivity and conformational control of cyclic tetrapeptides derived from aziridine-containing amino acids
por: Chung, Benjamin K. W., et al.
Publicado: (2016) -
Mechanistic study of styrene aziridination by iron(iv) nitrides
por: Crandell, Douglas W., et al.
Publicado: (2018) -
Macrocycles: lessons from the distant past, recent developments, and future directions
por: Yudin, Andrei K.
Publicado: (2015) -
Introduction to ‘Synthesis and chemical biology of macrocycles’
por: Chen, Gong, et al.
Publicado: (2022) -
Asymmetric [3 + 2] cycloaddition of donor–acceptor aziridines with aldehydes via carbon–carbon bond cleavage
por: Liao, Yuting, et al.
Publicado: (2016)