Regio- and stereoselective synthesis of 1→6 linked manno-, gluco-, and galactopyranose Di-, Tri-, and tetrasaccharides via orthoester intermediates

Article abstract of DOI:10.1080/07328300008544122

1→6 linked manno-, gluco-, and galactopyranose di-, tri-, and tetrasaccharides with 1,2-trans glycosidic linkages were concisely and effectively synthesized using peracetylated glycosyl bromides as the donors and unprotected or partially protected glycopy

Full text of DOI:10.1080/07328300008544122

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Journal of Carbohydrate Chemistry
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Regio- and Stereoselective Synthesis
of 1→6 Linked Manno-, Gluco-,
and Galactopyranose Di-, Tri-, and
Tetrasaccharides Via Orthoester
Intermediates
Yuliang Zhu & Fanzuo Kong
a Research Center for Eco-Environmental Science, Academia
Sinica, P.O.Box 2871, Beijing 100085, China
b Research Center for Eco-Environmental Science, Academia
Sinica, P.O.Box 2871, Beijing 100085, China
Published online: 27 Feb 2008.
To cite this article: Yuliang Zhu & Fanzuo Kong (2000) Regio- and Stereoselective Synthesis
of 1→6 Linked Manno-, Gluco-, and Galactopyranose Di-, Tri-, and Tetrasaccharides
Via Orthoester Intermediates, Journal of Carbohydrate Chemistry, 19:7, 837-848, DOI:
10.1080/07328300008544122
To link to this article: http://dx.doi.org/10.1080/07328300008544122
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