| pubmed-article:19290359 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19290359 | lifeskim:mentions | umls-concept:C0204727 | lld:lifeskim |
| pubmed-article:19290359 | lifeskim:mentions | umls-concept:C0205409 | lld:lifeskim |
| pubmed-article:19290359 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:19290359 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:19290359 | lifeskim:mentions | umls-concept:C0205360 | lld:lifeskim |
| pubmed-article:19290359 | lifeskim:mentions | umls-concept:C0054666 | lld:lifeskim |
| pubmed-article:19290359 | pubmed:issue | 13 | lld:pubmed |
| pubmed-article:19290359 | pubmed:dateCreated | 2009-3-17 | lld:pubmed |
| pubmed-article:19290359 | pubmed:abstractText | A chiral seven-membered N-heterocyclic carbene (NHC) has been synthesized from its phenol adduct (NHC-HOPh) by a novel base-induced alpha-elimination method, and its donor strength has been determined from the IR stretching frequencies of the NHC-Rh(CO)(2)Cl complex. | lld:pubmed |
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| pubmed-article:19290359 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19290359 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19290359 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:19290359 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19290359 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19290359 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:19290359 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19290359 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19290359 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:19290359 | pubmed:issn | 1477-9226 | lld:pubmed |
| pubmed-article:19290359 | pubmed:author | pubmed-author:GuzeiIlia AIA | lld:pubmed |
| pubmed-article:19290359 | pubmed:author | pubmed-author:StahlShannon... | lld:pubmed |
| pubmed-article:19290359 | pubmed:author | pubmed-author:ScarboroughCh... | lld:pubmed |
| pubmed-article:19290359 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:19290359 | pubmed:day | 7 | lld:pubmed |
| pubmed-article:19290359 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19290359 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19290359 | pubmed:pagination | 2284-6 | lld:pubmed |
| pubmed-article:19290359 | pubmed:dateRevised | 2010-12-3 | lld:pubmed |
| pubmed-article:19290359 | pubmed:meshHeading | pubmed-meshheading:19290359... | lld:pubmed |
| pubmed-article:19290359 | pubmed:meshHeading | pubmed-meshheading:19290359... | lld:pubmed |
| pubmed-article:19290359 | pubmed:meshHeading | pubmed-meshheading:19290359... | lld:pubmed |
| pubmed-article:19290359 | pubmed:meshHeading | pubmed-meshheading:19290359... | lld:pubmed |
| pubmed-article:19290359 | pubmed:meshHeading | pubmed-meshheading:19290359... | lld:pubmed |
| pubmed-article:19290359 | pubmed:meshHeading | pubmed-meshheading:19290359... | lld:pubmed |
| pubmed-article:19290359 | pubmed:meshHeading | pubmed-meshheading:19290359... | lld:pubmed |
| pubmed-article:19290359 | pubmed:meshHeading | pubmed-meshheading:19290359... | lld:pubmed |
| pubmed-article:19290359 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19290359 | pubmed:articleTitle | Synthesis and isolation of a stable, axially-chiral seven-membered N-heterocyclic carbene. | lld:pubmed |
| pubmed-article:19290359 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19290359 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:19290359 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
