Selective electrochemical glycosylation by reactivity tuning.
Electrochemical glycosylation of a selenoglycoside donor proceeds efficiently in an undivided cell in acetonitrile to yield beta-glycosides. Measurement of cyclic voltammograms for a selection of seleno-, thio-, and O-glycosides indicates the dependence of oxidation potential on the anomeric substit...
المؤلفون الرئيسيون: | France, R, Compton, R, Davis, B, Fairbanks, A, Rees, N, Wadhawan, J |
---|---|
التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2004
|
مواد مشابهة
-
Selective activation of glycosyl donors utilising electrochemical techniques: a study of the thermodynamic oxidation potentials of a range of chalcoglycosides.
حسب: France, R, وآخرون
منشور في: (2004) -
Protecting group and solvent effects in electrochemical glycosylation
حسب: Drouin, L, وآخرون
منشور في: (2007) -
Electrochemical glycosylation in the presence of a catalytic chemical mediator
حسب: Drouin, L, وآخرون
منشور في: (2008) -
Peptide templated glycosylation reactions
حسب: Tennant-Eyles, R, وآخرون
منشور في: (2000) -
An electrochemical study of the oxidation of 1.3,5-Tris[4-[(3-methylphenyl)phenylamino]phenyl]benzene
حسب: Rees, N, وآخرون
منشور في: (2004)