pubmed-article:19277363 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19277363 | lifeskim:mentions | umls-concept:C0014442 | lld:lifeskim |
pubmed-article:19277363 | lifeskim:mentions | umls-concept:C0020291 | lld:lifeskim |
pubmed-article:19277363 | lifeskim:mentions | umls-concept:C0002068 | lld:lifeskim |
pubmed-article:19277363 | lifeskim:mentions | umls-concept:C1705294 | lld:lifeskim |
pubmed-article:19277363 | lifeskim:mentions | umls-concept:C0332514 | lld:lifeskim |
pubmed-article:19277363 | lifeskim:mentions | umls-concept:C0075804 | lld:lifeskim |
pubmed-article:19277363 | pubmed:issue | 12 | lld:pubmed |
pubmed-article:19277363 | pubmed:dateCreated | 2009-3-11 | lld:pubmed |
pubmed-article:19277363 | pubmed:abstractText | Chiral aryl vicinal diols were obtained in high ee and yield by asymmetric dihydroxylation of aryl olefins with tandem biocatalysts: one contains an enantioselective styrene monooxygenase, and the other contains a regioselective epoxide hydrolase. | lld:pubmed |
pubmed-article:19277363 | pubmed:language | eng | lld:pubmed |
pubmed-article:19277363 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19277363 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:19277363 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19277363 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19277363 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19277363 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19277363 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19277363 | pubmed:month | Mar | lld:pubmed |
pubmed-article:19277363 | pubmed:issn | 1359-7345 | lld:pubmed |
pubmed-article:19277363 | pubmed:author | pubmed-author:GoMMJr | lld:pubmed |
pubmed-article:19277363 | pubmed:author | pubmed-author:JinXiaX | lld:pubmed |
pubmed-article:19277363 | pubmed:author | pubmed-author:LiZhiZ | lld:pubmed |
pubmed-article:19277363 | pubmed:author | pubmed-author:PankeSvenS | lld:pubmed |
pubmed-article:19277363 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:19277363 | pubmed:day | 28 | lld:pubmed |
pubmed-article:19277363 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19277363 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19277363 | pubmed:pagination | 1481-3 | lld:pubmed |
pubmed-article:19277363 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
pubmed-article:19277363 | pubmed:meshHeading | pubmed-meshheading:19277363... | lld:pubmed |
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pubmed-article:19277363 | pubmed:meshHeading | pubmed-meshheading:19277363... | lld:pubmed |
pubmed-article:19277363 | pubmed:meshHeading | pubmed-meshheading:19277363... | lld:pubmed |
pubmed-article:19277363 | pubmed:meshHeading | pubmed-meshheading:19277363... | lld:pubmed |
pubmed-article:19277363 | pubmed:meshHeading | pubmed-meshheading:19277363... | lld:pubmed |
pubmed-article:19277363 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19277363 | pubmed:articleTitle | Asymmetric dihydroxylation of aryl olefins by sequential enantioselective epoxidation and regioselective hydrolysis with tandem biocatalysts. | lld:pubmed |
pubmed-article:19277363 | pubmed:affiliation | Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore 117576. | lld:pubmed |
pubmed-article:19277363 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19277363 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |