The synthesis of 2,2,3,3-tetrafluorinated galactose and glucose derivatives
The incorporation of polyfluorinated regions into carbohydrates has been proposed as a strategy to improve the typically low protein–carbohydrate affinity. The creation of a hydrophobic region, while maintaining a potential for attractive dipolar interactions (mediated by the polarised C–F bond) may...
Main Author: | Golten, Samuel |
---|---|
Other Authors: | Linclau, Bruno |
Published: |
University of Southampton
2012
|
Subjects: | |
Online Access: | https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581472 |
Similar Items
-
The enantioselective synthesis of 2,3-dideoxy-2,2,3,3-tetrafluoro-galactose and 2,3-dideoxy-2,2,3,3-tetrafluoro-glucose
by: Timofte, Roxana Sidonia
Published: (2007) -
The molecular structure of galactose-containing polysaccharides of the plant gum and hemi-cellulose groups
by: Nicolson, A.
Published: (1959) -
Solid-phase synthesis of carbohydrate derivatives
by: Rice, David Cunningham
Published: (2000) -
Synthesis and studies of stannylated carbohydrate derivatives
by: Rufino, Helena Clara de Assuncao Rufino
Published: (1998) -
1,2-metallate rearrangement of carbohydrate derivatives
by: Komsta, Zofia Aleksandra
Published: (2010)