Cargando…
Stereoselectivity of Conformationally Restricted Glucosazide Donors
[Image: see text] Glycosylations of 4,6-tethered glucosazide donors with a panel of model acceptors revealed the effect of acceptor nucleophilicity on the stereoselectivity of these donors. The differences in reactivity among the donors were evaluated in competitive glycosylation reactions, and thei...
Autores principales: | van der Vorm, Stefan, Overkleeft, Herman S., van der Marel, Gijsbert A., Codée, Jeroen D. C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423080/ https://www.ncbi.nlm.nih.gov/pubmed/28401764 http://dx.doi.org/10.1021/acs.joc.7b00470 |
Ejemplares similares
-
Mapping the Relationship between Glycosyl Acceptor Reactivity and Glycosylation Stereoselectivity
por: van der Vorm, Stefan, et al.
Publicado: (2018) -
Reagent
Controlled Stereoselective Synthesis of α-Glucans
por: Wang, Liming, et al.
Publicado: (2018) -
Reagent Controlled Stereoselective Assembly of α‐(1,3)‐Glucans
por: Wang, Liming, et al.
Publicado: (2018) -
Furanosyl Oxocarbenium Ion Conformational Energy Landscape Maps as a Tool to Study the Glycosylation Stereoselectivity of 2‐Azidofuranoses, 2‐Fluorofuranoses and Methyl Furanosyl Uronates
por: van der Vorm, Stefan, et al.
Publicado: (2019) -
Synthesis, Reactivity,
and Stereoselectivity of 4-Thiofuranosides
por: Madern, Jerre M., et al.
Publicado: (2019)