Cargando…
Inverting Small Molecule–Protein Recognition by the Fluorine Gauche Effect: Selectivity Regulated by Multiple H→F Bioisosterism
Fluorinated motifs have a venerable history in drug discovery, but as C(sp(3))−F‐rich 3D scaffolds appear with increasing frequency, the effect of multiple bioisosteric changes on molecular recognition requires elucidation. Herein we demonstrate that installation of a 1,3,5‐stereotriad, in the subst...
Autores principales: | Bentler, Patrick, Bergander, Klaus, Daniliuc, Constantin G., Mück‐Lichtenfeld, Christian, Jumde, Ravindra P., Hirsch, Anna K. H., Gilmour, Ryan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771710/ https://www.ncbi.nlm.nih.gov/pubmed/31157945 http://dx.doi.org/10.1002/anie.201905452 |
Ejemplares similares
-
Can acyclic conformational control be achieved via a sulfur–fluorine gauche effect?
por: Thiehoff, C., et al.
Publicado: (2015) -
Conformational Analysis of Acyclic α‐Fluoro Sulfur Motifs
por: Erdeljac, Nathalie, et al.
Publicado: (2020) -
Accessing (Multi)Fluorinated Piperidines Using Heterogeneous
Hydrogenation
por: Wagener, Tobias, et al.
Publicado: (2020) -
Trifluorinated Tetralins via I(I)/I(III)‐Catalysed Ring Expansion: Programming Conformation by [CH(2)CH(2)] → [CF(2)CHF] Isosterism
por: Neufeld, Jessica, et al.
Publicado: (2021) -
Regioselective, catalytic 1,1-difluorination of enynes
por: Wang, Zi-Xuan, et al.
Publicado: (2023)