Cargando…
Protecting group free glycosylation: one-pot stereocontrolled access to 1,2-trans glycosides and (1→6)-linked disaccharides of 2-acetamido sugars
Unprotected 2-acetamido sugars may be directly converted into their oxazolines using 2-chloro-1,3-dimethylimidazolinium chloride (DMC), and a suitable base, in aqueous solution. Freeze drying and acid catalysed reaction with an alcohol as solvent produces the corresponding 1,2-trans-glycosides in go...
Autores principales: | Qiu, Xin, Garden, Anna L., Fairbanks, Antony J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8985506/ https://www.ncbi.nlm.nih.gov/pubmed/35440979 http://dx.doi.org/10.1039/d2sc00222a |
Ejemplares similares
-
Stereocontrolled Synthesis of 2‐Fluorinated C‐Glycosides
por: Sadurní, Anna, et al.
Publicado: (2018) -
Sugar silanes: versatile reagents for stereocontrolled glycosylation via intramolecular aglycone delivery
por: Walk, Jordan T., et al.
Publicado: (2015) -
Stereocontrolled 1,2-cis glycosylation as the driving force of progress in synthetic carbohydrate chemistry
por: Nigudkar, Swati S., et al.
Publicado: (2015) -
Stereocontrolled Synthesis and Conformational Analysis of a Series of Disaccharides α,β-d-GlcA-(1→3)-α-L-Fuc
por: Gerbst, Alexey G., et al.
Publicado: (2023) -
Organocatalytic one-pot 1,4-/1,6-/1,2-addition sequence for the stereocontrolled formation of six consecutive stereocenters
por: Chauhan, Pankaj, et al.
Publicado: (2015)