In situ F-19 NMR spectroscopy study of enzymatic transglycosylation reactions using alpha-D-aldohexopyranosyl fluorides as donors and accepters

Citation
C. Andre et al., In situ F-19 NMR spectroscopy study of enzymatic transglycosylation reactions using alpha-D-aldohexopyranosyl fluorides as donors and accepters, TETRAHEDR-A, 12(5), 2001, pp. 779-783
Citations number
23
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON-ASYMMETRY
ISSN journal
09574166 → ACNP
Volume
12
Issue
5
Year of publication
2001
Pages
779 - 783
Database
ISI
SICI code
0957-4166(20010402)12:5<779:ISFNSS>2.0.ZU;2-E
Abstract
The use of F-19 NMR spectroscopy to study the kinetics of the self-condensa tion reaction of alpha -D-aldohexopyranosyl fluorides catalysed by alpha -g lycosidases is described. The corresponding fluorinated disaccharides thus: synthesised present separate individual fluorine resonances allowing the i ntegration of each species. This method looks particularly useful to help i n the choice of donor in enzymatic transglycosylation reactions since the s elf-condensation reaction always remains in competition with the condensati on reaction (reaction of the donor with accepters other than itself). (C) 2 001 Elsevier Science Ltd. All rights reserved.