Stereoselective oxidative glycosylation of anomeric nucleophiles with alcohols and carboxylic acids
Glycosylation of partially protected sugars is usually limited by suboptimal regio- and stereo-selectivities. Here, the authors show a general oxidative glycosylation between anomeric stannanes with a nonprotected hydroxyl group and oxygen nucleophiles, additionally providing mechanistic insights in...
Guardado en:
Autores principales: | Tianyi Yang, Feng Zhu, Maciej A. Walczak |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2018
|
Materias: | |
Acceso en línea: | https://doaj.org/article/bd44fa52016a458d892177d7d8de54c4 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
A minimalist approach to stereoselective glycosylation with unprotected donors
por: Kim Le Mai Hoang, et al.
Publicado: (2017) -
Impact of Carboxyl Groups in Graphene Oxide on Chemoselective Alcohol Oxidation with Ultra-Low Carbocatalyst Loading
por: Yan Cui, et al.
Publicado: (2017) -
Synthesis of Sulfo-Sialic Acid Analogues: Potent Neuraminidase Inhibitors in Regards to Anomeric Functionality
por: Christopher J. Vavricka, et al.
Publicado: (2017) -
Synthesis of triarylpyridines with sulfonate and sulfonamide moieties via a cooperative vinylogous anomeric-based oxidation
por: Morteza Torabi, et al.
Publicado: (2021) -
Catalytic enantioselective oxidative coupling of saturated ethers with carboxylic acid derivatives
por: Gang Wang, et al.
Publicado: (2019)