| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1388589 | Carbohydrate Research | 2008 | 7 Pages |
Abstract
Galactofuranose metabolism is a good target for the development of novel chemotherapeutic agents for the treatment of some microbial infections. A simple procedure for the synthesis of methyl (methyl α,β-d-galactopyranosid)uronate followed by NaB3H4 reduction gave a straightforward access to radiolabeled substrates for galactofuranosidases.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Facile synthesis of methyl α- and β-d-[6-3H]galactofuranosides from d-galacturonic acid. Substrates for the detection of galactofuranosidases](/preview/png/1388589.png "First Page Preview: Facile synthesis of methyl α- and β-d-[6-3H]galactofuranosides from d-galacturonic acid. Substrates for the detection of galactofuranosidases")
Authors
Andrea Bordoni, Carlos Lima, Karina Mariño, Rosa M. de Lederkremer, Carla Marino,