Reagent-controlled regiodivergent ring expansions of steroids
Late-stage diversification of natural products is an important starting point for drug discovery. Here, the authors use chiral reagents to perform the regiocontrolled ring expansion of steroid precursors and achieve more than 100 isomerically pure analogs with spatial and functional diversity.
Guardado en:
Autores principales: | Manwika Charaschanya, Jeffrey Aubé |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2018
|
Materias: | |
Acceso en línea: | https://doaj.org/article/c474749e5c3742fcb1e3a9c7bde664bc |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Integrated catalysis opens new arylation pathways via regiodivergent enzymatic C–H activation
por: Jonathan Latham, et al.
Publicado: (2016) -
Quality control of protein reagents for the improvement of research data reproducibility
por: Ario de Marco, et al.
Publicado: (2021) -
Steroid hormone bioavailability is controlled by the lymphatic system
por: Rahel Klossner, et al.
Publicado: (2021) -
Polysulfurating reagent design for unsymmetrical polysulfide construction
por: Xiao Xiao, et al.
Publicado: (2018) -
Photons as a 21st century reagent
por: Holly E. Bonfield, et al.
Publicado: (2020)