Prearranged glycosides. Part 8. Intramolecular α-galactosylation via succinoyl tethered glycosides

Article abstract of DOI:10.1080/07328309908544056

Benzyl protected phenyl 1-thio-galactopyranoside donors which were tethered by a succinoyl linker at their positions 2 and 6, respectively, to position 3 of a blocked benzyl glucopyranoside acceptor with a 4-OH group solely afforded the corresponding α-(1→4)-linked disaccharides upon intramolecular glycosylation. 4,6-Siloxane protected mannosides react with rearrangement of the siloxane group under similar conditions.

Full text of DOI:10.1080/07328309908544056

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Journal of Carbohydrate Chemistry
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Prearranged Glycosides. Part 8.
Intramolecular α-Galactosylation Via
Succinoyl Tethered Glycosides
Thomas Ziegler , Ralf Dettmann , Ariffadhillah & Uwe Zettl
a Institute of Organic Chemistry, University of Cologne ,
Greinstraße 4, D-50939 Cologne, Germany
b Institute of Organic Chemistry, University of Cologne ,
Greinstraße 4, D-50939 Cologne, Germany
c Institute of Organic Chemistry, University of Cologne ,
Greinstraße 4, D-50939 Cologne, Germany
d Institute of Organic Chemistry, University of Cologne ,
Greinstraße 4, D-50939 Cologne, Germany
Published online: 27 Feb 2008.
To cite this article: Thomas Ziegler , Ralf Dettmann , Ariffadhillah & Uwe Zettl
(1999) Prearranged Glycosides. Part 8. Intramolecular α-Galactosylation Via Succinoyl
Tethered Glycosides, Journal of Carbohydrate Chemistry, 18:9, 1079-1095, DOI:
10.1080/07328309908544056
To link to this article: http://dx.doi.org/10.1080/07328309908544056
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