Source:http://linkedlifedata.com/resource/pubmed/id/20924955
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2010-10-6
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pubmed:abstractText |
Tert-butyldiphenylsilyl (TBDPS) was testified to be an appropriate orthogonal protecting group for novel 7-hydroxyl-functionalized 8-aza-7-deaza-2'-deoxyadenosine analogues. It was stable in partial and complete hydrogenation reactions used for the different linker preparation. The corresponding phosphoramidites and hydroxyl-functionalized oligodeoxynucleotides were synthesized and identified. The thermal effect of the hydroxyl group with different linkers on DNA duplexes was evaluated. It provided a feasible strategy for the preparation of hydroxyl-functionalized DNAs for the nucleic acid research.
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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 |
Oct
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pubmed:issn |
1532-2335
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
29
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
734-47
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pubmed:meshHeading |
pubmed-meshheading:20924955-Base Pairing,
pubmed-meshheading:20924955-Base Sequence,
pubmed-meshheading:20924955-DNA Adducts,
pubmed-meshheading:20924955-Hydroxides,
pubmed-meshheading:20924955-Models, Molecular,
pubmed-meshheading:20924955-Nucleic Acid Denaturation,
pubmed-meshheading:20924955-Transition Temperature
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pubmed:year |
2010
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pubmed:articleTitle |
Hydroxyl-functionalized DNAs with different linkers and their complementary duplex stability.
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pubmed:affiliation |
School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang, P. R. China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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