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Synthesis 2005(6): 939-944
DOI: 10.1055/s-2005-861828
DOI: 10.1055/s-2005-861828
PAPER
© Georg Thieme Verlag Stuttgart · New York
New Synthesis of Mannoside-Containing Neoglycoconjugates by Reaction of Propargyl Mannosides with Polyalkylcarboxylated Scaffolds
Weitere Informationen
Received
24 September 2004
Publikationsdatum:
21. Februar 2005 (online)
Publikationsverlauf
Publikationsdatum:
21. Februar 2005 (online)
Abstract
A new, efficient and easy synthesis of multivalent mannoside neoglyconjugates is described by the alkynylation reaction of lithium acetylides derived from adequately protected propargyl α-d-mannoside and readily available polyalkylcarboxylate benzene derivatives as scaffolds.
Key words
glycosides - neoglycoconjugates - clusters - alkynes - polyalkylcarboxylates
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References
2-Propynyl α-d-mannopyranoside was synthesized from per-O-acetyl α-d-mannopyranoside and propargyl alcohol following the procedure described by Mereyala et al. [20]