| pubmed-article:16800022 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16800022 | lifeskim:mentions | umls-concept:C1510411 | lld:lifeskim |
| pubmed-article:16800022 | lifeskim:mentions | umls-concept:C0017945 | lld:lifeskim |
| pubmed-article:16800022 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:16800022 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:16800022 | lifeskim:mentions | umls-concept:C0332516 | lld:lifeskim |
| pubmed-article:16800022 | lifeskim:mentions | umls-concept:C0205250 | lld:lifeskim |
| pubmed-article:16800022 | lifeskim:mentions | umls-concept:C2699744 | lld:lifeskim |
| pubmed-article:16800022 | lifeskim:mentions | umls-concept:C0332514 | lld:lifeskim |
| pubmed-article:16800022 | pubmed:issue | 23 | lld:pubmed |
| pubmed-article:16800022 | pubmed:dateCreated | 2006-8-25 | lld:pubmed |
| pubmed-article:16800022 | pubmed:abstractText | Highly efficient synthesis of enantiopure diacetates of 2,4-pentanediol and 2,5-hexanediol starting from commercially available mixtures of the diols (dl/meso approximately 1:1) has been realized by combining a fast ruthenium-catalyzed epimerization with an enzymatic transesterification. The in situ coupling of these two processes produces the diacetates in high yield in >99 % enantiomeric excess. | lld:pubmed |
| pubmed-article:16800022 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16800022 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16800022 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:16800022 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16800022 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16800022 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16800022 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16800022 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16800022 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16800022 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16800022 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16800022 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:16800022 | pubmed:issn | 0947-6539 | lld:pubmed |
| pubmed-article:16800022 | pubmed:author | pubmed-author:BäckvallJan-E... | lld:pubmed |
| pubmed-article:16800022 | pubmed:author | pubmed-author:EdinMichaelaM | lld:pubmed |
| pubmed-article:16800022 | pubmed:author | pubmed-author:Martín-Matute... | lld:pubmed |
| pubmed-article:16800022 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16800022 | pubmed:day | 7 | lld:pubmed |
| pubmed-article:16800022 | pubmed:volume | 12 | lld:pubmed |
| pubmed-article:16800022 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16800022 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16800022 | pubmed:pagination | 6053-61 | lld:pubmed |
| pubmed-article:16800022 | pubmed:dateRevised | 2009-8-4 | lld:pubmed |
| pubmed-article:16800022 | pubmed:meshHeading | pubmed-meshheading:16800022... | lld:pubmed |
| pubmed-article:16800022 | pubmed:meshHeading | pubmed-meshheading:16800022... | lld:pubmed |
| pubmed-article:16800022 | pubmed:meshHeading | pubmed-meshheading:16800022... | lld:pubmed |
| pubmed-article:16800022 | pubmed:meshHeading | pubmed-meshheading:16800022... | lld:pubmed |
| pubmed-article:16800022 | pubmed:meshHeading | pubmed-meshheading:16800022... | lld:pubmed |
| pubmed-article:16800022 | pubmed:meshHeading | pubmed-meshheading:16800022... | lld:pubmed |
| pubmed-article:16800022 | pubmed:meshHeading | pubmed-meshheading:16800022... | lld:pubmed |
| pubmed-article:16800022 | pubmed:meshHeading | pubmed-meshheading:16800022... | lld:pubmed |
| pubmed-article:16800022 | pubmed:meshHeading | pubmed-meshheading:16800022... | lld:pubmed |
| pubmed-article:16800022 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16800022 | pubmed:articleTitle | Highly efficient synthesis of enantiopure diacetylated C(2)-symmetric diols by ruthenium- and enzyme-catalyzed dynamic kinetic asymmetric transformation (DYKAT). | lld:pubmed |
| pubmed-article:16800022 | pubmed:affiliation | Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, 10691 Stockholm, Sweden. | lld:pubmed |
| pubmed-article:16800022 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16800022 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
