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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
27
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pubmed:dateCreated |
1993-3-25
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pubmed:abstractText |
Pyrimidine nucleosides (or their 5'-aldehydes) when treated with DAST give O2,5'-(fluoro)-anhydronucleosides. If this is prevented by blocking N-3 or O4, the desired 5'-deoxy-5'-(di)-fluoronucleoside is accompanied by the production of a compound resulting from migration of the base following scission of the N-1-->C-1' bond and formation of O2-->C-5'. This is a particular example of a much more general phenomenon, seen when suitably substituted ribofuranoses are treated with DAST.
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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/Diethylamines,
http://linkedlifedata.com/resource/pubmed/chemical/Fluorine,
http://linkedlifedata.com/resource/pubmed/chemical/Indicators and Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrimidine Nucleosides,
http://linkedlifedata.com/resource/pubmed/chemical/diethylaminosulfur trifluoride
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pubmed:status |
MEDLINE
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pubmed:issn |
0261-3166
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
185-6
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pubmed:dateRevised |
2000-12-18
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pubmed:meshHeading | |
pubmed:year |
1992
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pubmed:articleTitle |
Some novel pyrimidine nucleoside rearrangements effected by diethylaminosulfur trifluoride (DAST).
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pubmed:affiliation |
School of Chemistry, University of Birmingham, UK.
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pubmed:publicationType |
Journal Article
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