Regio- and stereoselective synthesis of oligosaccharides with acetobromolactose and acetobromomaltose as glycosyl donors via orthoester intermediates

Article abstract of DOI:10.1080/07328309908544009

Regio- and stereoselective synthesis of some trisaccharides was effected in high yields from coupling of acetobromolactose or acetobromomaltose as donors with partially protected glucoside acceptors through an orthoester formation-rearrangement strategy. Selective 1→6 or 1→3 with 1,2-trans glycosylation was achieved.

Full text of DOI:10.1080/07328309908544009

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Journal of Carbohydrate Chemistry
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Regio-and Stereoselective
Synthesis of Oligosaccharides
with Acetobromolactose and
Acetobromomaltose as Glycosyl
Donors Via Orthoester Intermediates
Wei Wang & Fanzuo Kong
a Research Center for Eco-Environmental Sciences, Academia
Sinica, P.O. Box 2871, Beijing 100085, China
b Research Center for Eco-Environmental Sciences, Academia
Sinica, P.O. Box 2871, Beijing 100085, China
Published online: 27 Feb 2008.
To cite this article: Wei Wang & Fanzuo Kong (1999) Regio-and Stereoselective Synthesis
of Oligosaccharides with Acetobromolactose and Acetobromomaltose as Glycosyl Donors
Via Orthoester Intermediates, Journal of Carbohydrate Chemistry, 18:4, 451-460, DOI:
10.1080/07328309908544009
To link to this article: http://dx.doi.org/10.1080/07328309908544009
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