| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1389293 | Carbohydrate Research | 2007 | 6 Pages |
Abstract
Practical protocols are described for a five-step conversion of d-glucuronolactone into α-d-arabino-2-ketoglucuronyl bromides, which due to their α-selective or β-specific glycosidation, and gluco- or manno-specific carbonyl reductions of the glucurono-2-ulosides formed, are expedient indirect donor substrates for the efficient introduction of α-d-GlcA or β-d-ManA residues.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Matthias Lergenmüller, Frieder W. Lichtenthaler,