Source:http://linkedlifedata.com/resource/pubmed/id/12943383
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
18
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pubmed:dateCreated |
2003-8-28
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pubmed:abstractText |
[reaction: see text] We report a new synthesis of trehalose analogs that involves the use of intramolecular aglycone delivery for stereoselective formation of the 1,1-alpha,alpha-glycosidic bond. The glycosylation reaction afforded the desired isomer exclusively and in good yield.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1523-7060
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
4
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3185-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:12943383-Carbohydrate Sequence,
pubmed-meshheading:12943383-Glycosides,
pubmed-meshheading:12943383-Glycosylation,
pubmed-meshheading:12943383-Isomerism,
pubmed-meshheading:12943383-Models, Chemical,
pubmed-meshheading:12943383-Molecular Sequence Data,
pubmed-meshheading:12943383-Oxidation-Reduction,
pubmed-meshheading:12943383-Trehalose
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pubmed:year |
2003
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pubmed:articleTitle |
Formation of 1,1-alpha,alpha-glycosidic bonds by intramolecular aglycone delivery. A convergent synthesis of trehalose.
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pubmed:affiliation |
Center for New Directions in Organic Synthesis, Department of Chemistry, University of California, Berkeley, California 94720-1460, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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