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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2008-7-14
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pubmed:abstractText |
A heterocyclic nucleoside analogue library of uracils N1 tethered to isoxazoles, isoxazolines, and triazoles and uracil N3 tethered to isoxazolines and isoxazoles was constructed by solid-phase organic synthesis. This strategy opens the way for the generation of small libraries of heterocyclic nucleoside analogues for biological screening.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1520-4774
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
526-33
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pubmed:meshHeading |
pubmed-meshheading:18553984-Chromatography, High Pressure Liquid,
pubmed-meshheading:18553984-Cyclization,
pubmed-meshheading:18553984-Isoxazoles,
pubmed-meshheading:18553984-Molecular Structure,
pubmed-meshheading:18553984-Nucleosides,
pubmed-meshheading:18553984-Polystyrenes,
pubmed-meshheading:18553984-Resins, Synthetic,
pubmed-meshheading:18553984-Triazoles,
pubmed-meshheading:18553984-Uracil
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pubmed:articleTitle |
Solid-phase synthesis of heterocyclic nucleoside analogues: substituted uracils tethered to isoxazoles, isoxazolines, and triazoles from a selenopolystyrene resin.
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pubmed:affiliation |
Department of Chemistry, Zhejiang University (Xixi Campus), Hangzhou 310028, P. R. China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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