Selectively deoxygenated derivatives of β-maltosyl-(1→4)-trehalose as biological probes. II. The synthesis of the 4-and 4?-monodeoxygenated analogues

Article abstract of DOI:10.1080/07328309608005691

Two derivatives of β-maltosyl-(1→4)-trehalose monodeoxygenated at positions 4 or 4? have been synthesized in [2+2] block syntheses. After the preparation of precursors with only one free hydroxyl group the deoxy function was introduced by a Barton-McCombi

Full text of DOI:10.1080/07328309608005691

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Journal of Carbohydrate Chemistry
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Selectively Deoxygenated Derivatives of
β-Maltosyl-(1→4)-Trehalose as Biological
Probes. II. the Synthesis of the 4- and
4′″-Monodeoxygenated Analogues
Hans Peter Wessel a , Marie-Claude Viaud a & Michel Trumtel a
a Pharma Division , Preclinical Research F.Hoffmann-La Roche Ltd ,
CH-4070, Basel, Switzerland
Published online: 22 Aug 2006.
To cite this article: Hans Peter Wessel , Marie-Claude Viaud & Michel Trumtel (1996) Selectively
Deoxygenated Derivatives of β-Maltosyl-(1→4)-Trehalose as Biological Probes. II. the Synthesis of the
4- and 4′″-Monodeoxygenated Analogues, Journal of Carbohydrate Chemistry, 15:7, 769-786, DOI:
10.1080/07328309608005691
To link to this article: http://dx.doi.org/10.1080/07328309608005691
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