| pubmed-article:14565441 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C0001383 | lld:lifeskim |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C0028621 | lld:lifeskim |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C0028953 | lld:lifeskim |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C0439851 | lld:lifeskim |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C0205390 | lld:lifeskim |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C0037633 | lld:lifeskim |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C1382100 | lld:lifeskim |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C1552596 | lld:lifeskim |
| pubmed-article:14565441 | lifeskim:mentions | umls-concept:C1947931 | lld:lifeskim |
| pubmed-article:14565441 | pubmed:issue | 5-8 | lld:pubmed |
| pubmed-article:14565441 | pubmed:dateCreated | 2003-10-20 | lld:pubmed |
| pubmed-article:14565441 | pubmed:abstractText | The synthesis of 3'- and 5'-O-levulinyl nucleosidic monomers through enzymatic acylation with acetonoxime levulinate is demonstrated. The acylation process takes place in one-step and use of expensive reagents, such as DMTrCl is avoided. The regioselectivity of the procedure makes it very convenient for acylated monomers required for solution phase synthesis of oligonucleotides. | lld:pubmed |
| pubmed-article:14565441 | pubmed:language | eng | lld:pubmed |
| pubmed-article:14565441 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14565441 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:14565441 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14565441 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14565441 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14565441 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14565441 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14565441 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14565441 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:14565441 | pubmed:issn | 1525-7770 | lld:pubmed |
| pubmed-article:14565441 | pubmed:author | pubmed-author:GarcíaJavierJ | lld:pubmed |
| pubmed-article:14565441 | pubmed:author | pubmed-author:FerreroMiguel... | lld:pubmed |
| pubmed-article:14565441 | pubmed:author | pubmed-author:FernándezSusa... | lld:pubmed |
| pubmed-article:14565441 | pubmed:author | pubmed-author:GotorVicenteV | lld:pubmed |
| pubmed-article:14565441 | pubmed:author | pubmed-author:SanghviYogesh... | lld:pubmed |
| pubmed-article:14565441 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:14565441 | pubmed:volume | 22 | lld:pubmed |
| pubmed-article:14565441 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:14565441 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:14565441 | pubmed:pagination | 1455-7 | lld:pubmed |
| pubmed-article:14565441 | pubmed:meshHeading | pubmed-meshheading:14565441... | lld:pubmed |
| pubmed-article:14565441 | pubmed:meshHeading | pubmed-meshheading:14565441... | lld:pubmed |
| pubmed-article:14565441 | pubmed:meshHeading | pubmed-meshheading:14565441... | lld:pubmed |
| pubmed-article:14565441 | pubmed:meshHeading | pubmed-meshheading:14565441... | lld:pubmed |
| pubmed-article:14565441 | pubmed:meshHeading | pubmed-meshheading:14565441... | lld:pubmed |
| pubmed-article:14565441 | pubmed:meshHeading | pubmed-meshheading:14565441... | lld:pubmed |
| pubmed-article:14565441 | pubmed:meshHeading | pubmed-meshheading:14565441... | lld:pubmed |
| pubmed-article:14565441 | pubmed:meshHeading | pubmed-meshheading:14565441... | lld:pubmed |
| pubmed-article:14565441 | pubmed:articleTitle | Direct regioselective enzymatic acylation of nucleosides: building-blocks for the solution phase synthesis of oligonucleotides. | lld:pubmed |
| pubmed-article:14565441 | pubmed:affiliation | Departamento de Química Orgánica e Inorgánica, Facultad de Química, Universidad de Oviedo, Oviedo, Spain. | lld:pubmed |
| pubmed-article:14565441 | pubmed:publicationType | Journal Article | lld:pubmed |
