Selectively deoxygenated derivatives of β-maltosyl-(1→4)-trehalose as biological probes

Article abstract of DOI:10.1080/07328309608005672

The four derivatives of β-maltosyl-(1→4)-trehalose have been synthesized, which are monodeoxygenated at the site of one of the primary hydroxyl groups. The tetrasaccharides were constructed in [2+2] block syntheses. Thus, 6?-deoxy-β-maltosyl-(1→4)-trehalo

Full text of DOI:10.1080/07328309608005672

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Journal of Carbohydrate Chemistry
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Selectively Deoxygenated Derivatives of
β-Maltosyl-(1→4)-Trehalose as Biological
Probes
Hans Peter Wessel a , Michel Trumtel a & Rudolf Minder a
a Pharma Division, Preclinical Research F.Hoffmann-La Roche Ltd,
CH-4002, Basel, Switzerland
Published online: 22 Aug 2006.
To cite this article: Hans Peter Wessel , Michel Trumtel & Rudolf Minder (1996): Selectively
Deoxygenated Derivatives of β-Maltosyl-(1→4)-Trehalose as Biological Probes, Journal of
Carbohydrate Chemistry, 15:5, 523-548
To link to this article: http://dx.doi.org/10.1080/07328309608005672
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