pubmed-article:19333485 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19333485 | lifeskim:mentions | umls-concept:C0007009 | lld:lifeskim |
pubmed-article:19333485 | lifeskim:mentions | umls-concept:C1524063 | lld:lifeskim |
pubmed-article:19333485 | lifeskim:mentions | umls-concept:C0079411 | lld:lifeskim |
pubmed-article:19333485 | lifeskim:mentions | umls-concept:C0205117 | lld:lifeskim |
pubmed-article:19333485 | lifeskim:mentions | umls-concept:C0205372 | lld:lifeskim |
pubmed-article:19333485 | lifeskim:mentions | umls-concept:C0332514 | lld:lifeskim |
pubmed-article:19333485 | pubmed:issue | 15 | lld:pubmed |
pubmed-article:19333485 | pubmed:dateCreated | 2009-3-31 | lld:pubmed |
pubmed-article:19333485 | pubmed:abstractText | Organocatalytic asymmetric Michael reactions of fluorinated nucleophiles with nitroolefins catalyzed by Cinchona alkaloid-derived thiourea catalysts generated the desired Michael products containing vicinal fluorinated quaternary and tertiary chiral centers with exceptional enantioselectivity. | lld:pubmed |
pubmed-article:19333485 | pubmed:language | eng | lld:pubmed |
pubmed-article:19333485 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19333485 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:19333485 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19333485 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19333485 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19333485 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19333485 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19333485 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19333485 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19333485 | pubmed:month | Apr | lld:pubmed |
pubmed-article:19333485 | pubmed:issn | 1359-7345 | lld:pubmed |
pubmed-article:19333485 | pubmed:author | pubmed-author:InEE | lld:pubmed |
pubmed-article:19333485 | pubmed:author | pubmed-author:HanXiaoX | lld:pubmed |
pubmed-article:19333485 | pubmed:author | pubmed-author:LiuChenC | lld:pubmed |
pubmed-article:19333485 | pubmed:author | pubmed-author:LuYixinY | lld:pubmed |
pubmed-article:19333485 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:19333485 | pubmed:day | 21 | lld:pubmed |
pubmed-article:19333485 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19333485 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19333485 | pubmed:pagination | 2044-6 | lld:pubmed |
pubmed-article:19333485 | pubmed:meshHeading | pubmed-meshheading:19333485... | lld:pubmed |
pubmed-article:19333485 | pubmed:meshHeading | pubmed-meshheading:19333485... | lld:pubmed |
pubmed-article:19333485 | pubmed:meshHeading | pubmed-meshheading:19333485... | lld:pubmed |
pubmed-article:19333485 | pubmed:meshHeading | pubmed-meshheading:19333485... | lld:pubmed |
pubmed-article:19333485 | pubmed:meshHeading | pubmed-meshheading:19333485... | lld:pubmed |
pubmed-article:19333485 | pubmed:meshHeading | pubmed-meshheading:19333485... | lld:pubmed |
pubmed-article:19333485 | pubmed:meshHeading | pubmed-meshheading:19333485... | lld:pubmed |
pubmed-article:19333485 | pubmed:meshHeading | pubmed-meshheading:19333485... | lld:pubmed |
pubmed-article:19333485 | pubmed:meshHeading | pubmed-meshheading:19333485... | lld:pubmed |
pubmed-article:19333485 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19333485 | pubmed:articleTitle | Asymmetric generation of fluorine-containing quaternary carbons adjacent to tertiary stereocenters: uses of fluorinated methines as nucleophiles. | lld:pubmed |
pubmed-article:19333485 | pubmed:affiliation | Department of Chemistry, National University of Singapore, Singapore, Republic of Singapore. | lld:pubmed |
pubmed-article:19333485 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19333485 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |