Cargando…
Structure–function relationships in aryl diazirines reveal optimal design features to maximize C–H insertion
Diazirine reagents allow for the ready generation of carbenes upon photochemical, thermal, or electrical stimulation. Because carbenes formed in this way can undergo rapid insertion into any nearby C–H, O–H or N–H bond, molecules that encode diazirine functions have emerged as privileged tools in ap...
Autores principales: | Musolino, Stefania F., Pei, Zhipeng, Bi, Liting, DiLabio, Gino A., Wulff, Jeremy E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457397/ https://www.ncbi.nlm.nih.gov/pubmed/34667579 http://dx.doi.org/10.1039/d1sc03631a |
Ejemplares similares
-
Flexible polyfluorinated bis-diazirines as molecular adhesives
por: Simhadri, Chakravarthi, et al.
Publicado: (2021) -
Emerging Applications of Aryl Trifluoromethyl Diazoalkanes
and Diazirines in Synthetic Transformations
por: Ollevier, Thierry, et al.
Publicado: (2022) -
Covalent functionalization of polypropylene filters with diazirine–photosensitizer conjugates producing visible light driven virus inactivating materials
por: Cuthbert, T. J., et al.
Publicado: (2021) -
Non-covalent interactions in quantum chemistry and physics: theory and applications
por: Roza, Alberto Otero de la, et al.
Publicado: (2017) -
Optimized Fragmentation Regime for Diazirine Photo-Cross-Linked
Peptides
por: Giese, Sven H., et al.
Publicado: (2016)