Source:http://linkedlifedata.com/resource/pubmed/id/11322725
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2001-4-26
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pubmed:abstractText |
Four neoglycolipids having 2-amino-2-deoxy-D-glucose or D-galactose moieties linked to the lipidic part by a glucitol or a mannitol spacer-arm have been synthesized. The key step of the synthetic strategy was the regiospecific or regioselective beta-glycosylation of partially protected glucitol or mannitol acceptors by either 3,4,6-tri-O-acetyl-2-deoxy-2-iodo-alpha-D-mannopyranosyl azide or 2,3,4,6-tetra-O-benzoyl-alpha-D-galactopyranosyl trichloroacetimidate donors.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Galactose,
http://linkedlifedata.com/resource/pubmed/chemical/Glucosamine,
http://linkedlifedata.com/resource/pubmed/chemical/Glycolipids,
http://linkedlifedata.com/resource/pubmed/chemical/Mannitol,
http://linkedlifedata.com/resource/pubmed/chemical/Sorbitol
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0008-6215
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
22
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pubmed:volume |
331
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
107-17
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pubmed:meshHeading | |
pubmed:year |
2001
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pubmed:articleTitle |
Syntheses of neoglycolipids with hexitol spacers between the saccharidic and the lipidic parts.
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pubmed:affiliation |
Laboratoire de Chimie Organique II, Unité Mixte de Recherche CNRS 5622, Université Lyon 1, Chimie Phyisique Electronique de Lyon, Villeurbanne, France. lafont@univ-lyon1.fr
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pubmed:publicationType |
Journal Article
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