| pubmed-article:12271672 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:12271672 | lifeskim:mentions | umls-concept:C0031428 | lld:lifeskim |
| pubmed-article:12271672 | lifeskim:mentions | umls-concept:C0038739 | lld:lifeskim |
| pubmed-article:12271672 | lifeskim:mentions | umls-concept:C0005036 | lld:lifeskim |
| pubmed-article:12271672 | lifeskim:mentions | umls-concept:C0030011 | lld:lifeskim |
| pubmed-article:12271672 | lifeskim:mentions | umls-concept:C0449444 | lld:lifeskim |
| pubmed-article:12271672 | lifeskim:mentions | umls-concept:C0075804 | lld:lifeskim |
| pubmed-article:12271672 | pubmed:issue | 17 | lld:pubmed |
| pubmed-article:12271672 | pubmed:dateCreated | 2002-9-25 | lld:pubmed |
| pubmed-article:12271672 | pubmed:abstractText | Dioxygenase-catalysed trioxygenation of alkyl phenyl sulfides and alkyl benzenes yields enantiopure cis-dihydrodiol sulfoxides and triols respectively; naphthalene cis-dihydrodiol dehydrogenase-catalysed aromatisation of these diastereoisomers gives enantiopure catechols of either configuration. | lld:pubmed |
| pubmed-article:12271672 | pubmed:language | eng | lld:pubmed |
| pubmed-article:12271672 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12271672 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:12271672 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12271672 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12271672 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12271672 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12271672 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12271672 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12271672 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:12271672 | pubmed:issn | 1359-7345 | lld:pubmed |
| pubmed-article:12271672 | pubmed:author | pubmed-author:DaltonHowardH | lld:pubmed |
| pubmed-article:12271672 | pubmed:author | pubmed-author:KulakovLeonid... | lld:pubmed |
| pubmed-article:12271672 | pubmed:author | pubmed-author:LarkinMichael... | lld:pubmed |
| pubmed-article:12271672 | pubmed:author | pubmed-author:BoydDerek RDR | lld:pubmed |
| pubmed-article:12271672 | pubmed:author | pubmed-author:SharmaNarain... | lld:pubmed |
| pubmed-article:12271672 | pubmed:author | pubmed-author:ShepherdSteve... | lld:pubmed |
| pubmed-article:12271672 | pubmed:author | pubmed-author:LjubezVeraV | lld:pubmed |
| pubmed-article:12271672 | pubmed:author | pubmed-author:ByrneBreige... | lld:pubmed |
| pubmed-article:12271672 | pubmed:author | pubmed-author:AllenChristop... | lld:pubmed |
| pubmed-article:12271672 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12271672 | pubmed:day | 7 | lld:pubmed |
| pubmed-article:12271672 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12271672 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12271672 | pubmed:pagination | 1914-5 | lld:pubmed |
| pubmed-article:12271672 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:12271672 | pubmed:meshHeading | pubmed-meshheading:12271672... | lld:pubmed |
| pubmed-article:12271672 | pubmed:meshHeading | pubmed-meshheading:12271672... | lld:pubmed |
| pubmed-article:12271672 | pubmed:meshHeading | pubmed-meshheading:12271672... | lld:pubmed |
| pubmed-article:12271672 | pubmed:meshHeading | pubmed-meshheading:12271672... | lld:pubmed |
| pubmed-article:12271672 | pubmed:meshHeading | pubmed-meshheading:12271672... | lld:pubmed |
| pubmed-article:12271672 | pubmed:meshHeading | pubmed-meshheading:12271672... | lld:pubmed |
| pubmed-article:12271672 | pubmed:meshHeading | pubmed-meshheading:12271672... | lld:pubmed |
| pubmed-article:12271672 | pubmed:meshHeading | pubmed-meshheading:12271672... | lld:pubmed |
| pubmed-article:12271672 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:12271672 | pubmed:articleTitle | Tandem enzyme-catalysed oxidations of alkyl phenyl sulfides and alkyl benzenes: enantiocomplementary routes to chiral phenols. | lld:pubmed |
| pubmed-article:12271672 | pubmed:affiliation | School of Chemistry, Queen's University of Belfast, Belfast, UK BT9 5AG. dr.boyd@qub.ac.uk | lld:pubmed |
| pubmed-article:12271672 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12271672 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
